Allele Registry

Canonical Allele Identifier: PA1139729793

Gene: LAMP2 HGNC NCBI

ClinVar RCV:

RCV001035811

ClinVar Variation:

835011

HGVS (amino-acid)	Matching Registered Transcripts
NP_054701.1:p.Val310Phe	CA414400262 NM_013995.2:c.928G>T