Canonical Allele Identifier: PA915979273
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 823986
ClinVar RCV Id: RCV001020718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Met140Ile
CA399089380
NM_001142571.2:c.420G>T
CA399089381
NM_001142571.2:c.420G>C
CA399089382
NM_001142571.2:c.420G>A