Canonical Allele Identifier: PA2829182113
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_001376536.1:p.Thr439Asn
CA2393068
NM_001389607.1:c.1316C>A