Canonical Allele Identifier: PA2829181048
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2470351
ClinVar RCV Id: RCV004263807
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376523.1:p.Val1407Met
CA2392409
NM_001389594.1:c.4219G>A