Canonical Allele Identifier: PA112160
Gene: CRADD HGNC NCBI

Linked Data

ClinVar Variation Id: 30360
ClinVar RCV Id: RCV000023305 RCV002285256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003796.1:p.Gly128Arg
CA129155
NM_003805.5:c.382G>C