Canonical Allele Identifier: PA2829391830
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 841553
ClinVar RCV Id: RCV001043804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg7Leu
CA400336251
NM_002876.4:c.20G>T