Allele Registry

Canonical Allele Identifier: PA2829374431

Gene: LAMP2 HGNC NCBI

ClinVar RCV:

RCV002037657

ClinVar Variation:

1452436

HGVS (amino-acid)	Matching Registered Transcripts
NP_002285.1:p.Val310Leu	CA414400263 NM_002294.3:c.928G>C