Canonical Allele Identifier: PA645499729
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 325651
ClinVar RCV Id: RCV000379376 RCV001352316 RCV001820979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Val63Met
CA8354903
NM_018081.2:c.187G>A