Canonical Allele Identifier: PA2829181774
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2371430
ClinVar RCV Id: RCV004212269
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376532.1:p.Thr540Asn
CA2393068
NM_001389603.1:c.1619C>A