Canonical Allele Identifier: PA195986
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 186828
ClinVar RCV Id: RCV000166479 RCV000409000 RCV000410543 RCV000657146 RCV001818392 RCV004528916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu297Pro
CA195984
NM_058216.3:c.890T>C