Canonical Allele Identifier: PA2573296704
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1379240
ClinVar RCV Id: RCV001914805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Tyr209Phe
CA400349440
NM_058216.3:c.626A>T