Canonical Allele Identifier: PA2580556592
Gene: USP51 HGNC NCBI

Linked Data

ClinVar Variation Id: 2473266
ClinVar RCV Id: RCV004266560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958443.1:p.His438Tyr
CA10429273
NM_201286.4:c.1312C>T