Canonical Allele Identifier: PA2830246070
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 230736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598332.1:p.Glu206Lys
CA10580438
NM_133629.3:c.616G>A