Canonical Allele Identifier: PA2825861267
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2835452
ClinVar RCV Id: RCV003687142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Asp140Gly
CA397859929
NM_001143990.2:c.419A>G