Canonical Allele Identifier: PA2829185156
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2976007
ClinVar RCV Id: RCV003834093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376596.1:p.Asp315His
CA3059171
NM_001389667.1:c.943G>C