Canonical Allele Identifier: PA342773
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 30976
ClinVar RCV Id: RCV000023967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.His376Tyr
CA342771
NM_018081.2:c.1126C>T