Canonical Allele Identifier: PA2829181438
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2457594
ClinVar RCV Id: RCV004248729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376528.1:p.Met1069Leu
CA2392644
NM_001389599.1:c.3205A>T
CA352735964
NM_001389599.1:c.3205A>C