NM_000129.4(F13A1):c.*627G>A AND Factor XIII, A subunit, deficiency of
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000353620.5
Allele description [Variation Report for NM_000129.4(F13A1):c.*627G>A]
NM_000129.4(F13A1):c.*627G>A
Condition(s)
- Name:
- Factor XIII, A subunit, deficiency of
- Synonyms:
- Factor XIII subunit A deficiency
- Identifiers:
- MONDO: MONDO:0013187; MedGen: C2750514; Orphanet: 331; OMIM: 613225; Human Phenotype Ontology: HP:0040233
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Last Updated: Apr 9, 2023