Canonical Allele Identifier: PA2829392057
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 246164
ClinVar RCV Id: RCV000236631 RCV000553107 RCV000564011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Glu45Asp
CA8677151
NM_002876.4:c.135G>C
CA400337748
NM_002876.4:c.135G>T