Allele Registry

Canonical Allele Identifier: PA2580349838

Gene: LAPTM5 HGNC NCBI

ClinVar RCV:

RCV004168791

ClinVar Variation:

2322885

HGVS (amino-acid)	Matching Registered Transcripts
NP_006753.1:p.Val84Ala	CA728106 NM_006762.3:c.251T>C