Canonical Allele Identifier: PA2829391852
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182842
ClinVar RCV Id: RCV000233682 RCV000587134 RCV000709500 RCV001189359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Gln11Arg
CA299901
NM_002876.4:c.32A>G