Canonical Allele Identifier: PA2825581662
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2803073
ClinVar RCV Id: RCV003622490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Ser155Gly
CA414402173
NM_001122606.1:c.463A>G