Canonical Allele Identifier: PA2825861907
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046088
ClinVar RCV Id: RCV001350597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Gly120Arg
CA8354940
NM_001143992.2:c.358G>A
CA397859003
NM_001143992.2:c.358G>C