Canonical Allele Identifier: PA2825861239
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716960
ClinVar RCV Id: RCV002297392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Asn101Lys
CA397858302
NM_001143990.2:c.303T>A
CA397858303
NM_001143990.2:c.303T>G