Canonical Allele Identifier: PA2829181326
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2371430
ClinVar RCV Id: RCV004212269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376527.1:p.Thr553Asn
CA2393068
NM_001389598.1:c.1658C>A