Canonical Allele Identifier: PA2829391829
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 480947
ClinVar RCV Id: RCV000563169 RCV000706180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg7His
CA292046832
NM_002876.4:c.20G>A