Allele Registry

Canonical Allele Identifier: PA120872

Gene: LAMP2 HGNC NCBI

ClinVar RCV:

RCV000010663

RCV000157981

RCV000844638

RCV002371769

ClinVar Variation:

9982

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116078.1:p.Val310Ile	CA120868 NM_001122606.1:c.928G>A