Canonical Allele Identifier: PA191977
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 185444
ClinVar RCV Id: RCV000164871 RCV000226827 RCV000587056 RCV001262192 RCV003150961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gly153Asp
CA191975
NM_058216.3:c.458G>A