Canonical Allele Identifier: PA104880
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 41252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Phe164Leu
CA344267
NM_001143990.2:c.492C>A
CA397860911
NM_001143990.2:c.490T>C
CA397860924
NM_001143990.2:c.492C>G