Canonical Allele Identifier: PA2825861580
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046088
ClinVar RCV Id: RCV001350597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137463.1:p.Gly120Arg
CA8354940
NM_001143991.2:c.358G>A
CA397859003
NM_001143991.2:c.358G>C