Canonical Allele Identifier: PA2829181979
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2534102
ClinVar RCV Id: RCV004310436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376534.1:p.Lys1136Arg
CA2392566
NM_001389605.1:c.3407A>G