Canonical Allele Identifier: PA2829392420
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142093
ClinVar RCV Id: RCV000130920 RCV000236213 RCV000197831 RCV001251311 RCV003462005 RCV003492606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Gly112Ala
CA333232
NM_002876.4:c.335G>C