Canonical Allele Identifier: PA2825861244
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1337779
ClinVar RCV Id: RCV001822377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Ser112Asn
CA8354935
NM_001143990.2:c.335G>A