Canonical Allele Identifier: PA2829374424
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2709050
ClinVar RCV Id: RCV003510732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Met303Leu
CA414400309
NM_002294.3:c.907A>T
CA414400310
NM_002294.3:c.907A>C