Canonical Allele Identifier: PA2829392220
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1789690
ClinVar RCV Id: RCV002448185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Thr78Ala
CA400340235
NM_002876.4:c.232A>G