Canonical Allele Identifier: PA164767
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 141205
ClinVar RCV Id: RCV000129608 RCV000411492 RCV000410493 RCV000986013
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr288Ala
CA164765
NM_058216.3:c.862A>G