Canonical Allele Identifier: PA288626
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128206
ClinVar RCV Id: RCV000116175 RCV000412269 RCV000199007 RCV001358061 RCV002267859 RCV000588889 RCV004556053 RCV003492509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Val169Ala
CA288624
NM_058216.3:c.506T>C