Canonical Allele Identifier: PA2829181900
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2534102
ClinVar RCV Id: RCV004310436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376533.1:p.Lys1187Arg
CA2392566
NM_001389604.1:c.3560A>G