Canonical Allele Identifier: PA2830153399
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2100018
ClinVar RCV Id: RCV003014200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Pro21Thr
CA400336775
NM_058216.3:c.61C>A