Canonical Allele Identifier: PA2827587307
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2534102
ClinVar RCV Id: RCV004310436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338027.1:p.Lys1175Arg
CA2392566
NM_001351098.2:c.3524A>G