Canonical Allele Identifier: PA2827040855
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_001307028.1:p.Gly128Arg
CA129155
NM_001320099.2:c.382G>C