Canonical Allele Identifier: PA2829391980
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 653924
ClinVar RCV Id: RCV000809784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Phe32Leu
CA400337240
NM_002876.4:c.94T>C
CA400337280
NM_002876.4:c.96C>A
CA400337284
NM_002876.4:c.96C>G