Canonical Allele Identifier: PA293925
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 138873
ClinVar RCV Id: RCV000128967 RCV000212967 RCV000588832 RCV001354814 RCV001723701 RCV000203773
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Glu233Gly
CA293923
NM_002878.4:c.698A>G