Canonical Allele Identifier: PA915979694
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Ile331Asn
CA287993
NM_001142571.2:c.992T>A