Canonical Allele Identifier: PA645460261
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409843
ClinVar RCV Id: RCV000472017 RCV003584610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ser231Leu
CA16615457
NM_058216.3:c.692C>T