Canonical Allele Identifier: PA2825861864
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373987
ClinVar RCV Id: RCV001877593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Gly48Arg
CA397856513
NM_001143992.2:c.142G>A
CA397856518
NM_001143992.2:c.142G>C