Canonical Allele Identifier: PA2827587488
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2556267
ClinVar RCV Id: RCV004325059
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338029.1:p.Gly1365Glu
CA352728636
NM_001351100.2:c.4094G>A