Canonical Allele Identifier: PA104869
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 30976
ClinVar RCV Id: RCV000023967
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.His376Tyr
CA342771
NM_001143990.2:c.1126C>T