Allele Registry

Canonical Allele Identifier: PA2827587802

Gene: USP19 HGNC NCBI

ClinVar RCV:

RCV004248729

ClinVar Variation:

2457594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338033.1:p.Met986Leu	CA2392644 NM_001351104.2:c.2956A>T CA352735964 NM_001351104.2:c.2956A>C