Canonical Allele Identifier: PA2829391931
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1370860
ClinVar RCV Id: RCV001878707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val23Met
CA400336857
NM_002876.4:c.67G>A