NM_000129.4(F13A1):c.749T>C (p.Leu250Pro) AND F13A1-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003969150.1
Allele description [Variation Report for NM_000129.4(F13A1):c.749T>C (p.Leu250Pro)]
NM_000129.4(F13A1):c.749T>C (p.Leu250Pro)
Condition(s)
- Name:
- F13A1-related disorder
- Synonyms:
- F13A1-related condition
- Identifiers:
-
eggc.vipEfA (0)
BioProject
-
eggc.vipLer (0)
BioProject
-
eggc.viphzb (0)
BioProject
-
eggc.vipU6M (0)
BioProject
-
-365 eggc.vipmz2 (35)
BioProject
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See more...Assertion and evidence details
Last Updated: May 26, 2024