Allele Registry

Canonical Allele Identifier: PA2829298438

Gene: USP19 HGNC NCBI

ClinVar RCV:

RCV004248729

ClinVar Variation:

2457594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387217.1:p.Met1085Leu	CA2392644 NM_001400288.1:c.3253A>T CA352735964 NM_001400288.1:c.3253A>C