Canonical Allele Identifier: PA2829391958
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 140837
ClinVar RCV Id: RCV000129034 RCV000552582 RCV001555080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Leu27Pro
CA163703
NM_002876.4:c.80T>C