Canonical Allele Identifier: PA190707
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 184991
ClinVar RCV Id: RCV000164342 RCV000227022 RCV000986011 RCV002465547 RCV003316020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His207Gln
CA190705
NM_058216.3:c.621T>A
CA400349394
NM_058216.3:c.621T>G