Canonical Allele Identifier: PA287961
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127883
ClinVar RCV Id: RCV000115809 RCV000204912 RCV000587212 RCV003150944 RCV000709452
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Ala49Val
CA287959
NM_002878.4:c.146C>T