Canonical Allele Identifier: PA2829928149
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3065121
ClinVar RCV Id: RCV003990198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061923.2:p.Val49Asp
CA358022181
NM_019050.3:c.146T>A