Canonical Allele Identifier: PA2829181155
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2405314
ClinVar RCV Id: RCV004237405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376525.1:p.Arg180His
CA2393359
NM_001389596.1:c.539G>A