NM_001278074.1(COL5A1):c.996C>T (p.Asp332=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000229492.3
Allele description
NM_001278074.1(COL5A1):c.996C>T (p.Asp332=)
Condition(s)
- Identifiers:
- MedGen: CN517202
-
Homo sapiens parathyroid hormone like hormone (PTHLH), transcript variant 3, mRN...
Homo sapiens parathyroid hormone like hormone (PTHLH), transcript variant 3, mRNAgi|39995088|ref|NM_198964.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Apr 18, 2020