Canonical Allele Identifier: PA2825800880
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 229719
ClinVar RCV Id: RCV000216942 RCV000534748 RCV001560841
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Ser227Pro
CA10580452
NM_001142571.2:c.679T>C