Canonical Allele Identifier: PA2829392024
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1391616
ClinVar RCV Id: RCV001893172 RCV004041430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Glu40Asp
CA400337588
NM_002876.4:c.120G>C
CA400337589
NM_002876.4:c.120G>T