Canonical Allele Identifier: PA645486283
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 234175
ClinVar RCV Id: RCV000217463 RCV000458645 RCV000709503 RCV001582758 RCV002467443
ClinVar Variation Id: 927230
ClinVar RCV Id: RCV001190352 RCV004033405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Trp135Ter
CA8677207
NM_002876.4:c.404G>A
CA8677208
NM_002876.4:c.405G>A