Allele Registry

Canonical Allele Identifier: PA2829181525

Gene: USP19 HGNC NCBI

ClinVar RCV:

RCV004248729

ClinVar Variation:

2457594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001376529.1:p.Met1068Leu	CA2392644 NM_001389600.1:c.3202A>T CA352735964 NM_001389600.1:c.3202A>C