Canonical Allele Identifier: PA2825861932
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 41252
ClinVar RCV Id: RCV000034152 RCV000439983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Phe164Leu
CA344267
NM_001143992.2:c.492C>A
CA397860911
NM_001143992.2:c.490T>C
CA397860924
NM_001143992.2:c.492C>G