Canonical Allele Identifier: PA288632
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128213
ClinVar RCV Id: RCV000116182 RCV003230405 RCV001854563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys320Arg
CA288630
NM_058216.3:c.959A>G