Canonical Allele Identifier: PA2829392374
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 627735
ClinVar Variation Id: 1377931
ClinVar RCV Id: RCV001880905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Phe103Leu
CA400341074
NM_002876.4:c.307T>C
CA400341098
NM_002876.4:c.309C>A
CA400341101
NM_002876.4:c.309C>G