Canonical Allele Identifier: PA658669074
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 472633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Asp326Ala
CA399086041
NM_002878.4:c.977A>C