Canonical Allele Identifier: PA2825861268
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338422
ClinVar RCV Id: RCV001817793
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Thr144Ser
CA397860086
NM_001143990.2:c.430A>T
CA397860090
NM_001143990.2:c.431C>G