Canonical Allele Identifier: PA915979324
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Asn158His
CA287974
NM_001142571.2:c.472A>C