Canonical Allele Identifier: PA165709
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 141532
ClinVar RCV Id: RCV000130100 RCV000462239 RCV000662674 RCV003441750 RCV003315885
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His179Gln
CA165707
NM_058216.3:c.537C>A
CA400345238
NM_058216.3:c.537C>G