Canonical Allele Identifier: PA2830474624
Gene: USP51 HGNC NCBI

Linked Data

ClinVar Variation Id: 3187758
ClinVar RCV Id: RCV004477601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958443.1:p.Gly12Ser
CA10429417
NM_201286.4:c.34G>A