Canonical Allele Identifier: PA2580498017
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1738822
ClinVar RCV Id: RCV002328033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Asp141His
CA400343853
NM_058216.3:c.421G>C