Canonical Allele Identifier: PA287995
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127896
ClinVar RCV Id: RCV000115822 RCV000233793 RCV000709427 RCV000656967 RCV001354391 RCV001818279 RCV003149804 RCV003492497
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Ile311Asn
CA287993
NM_002878.4:c.932T>A