Canonical Allele Identifier: PA2825581666
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949612
ClinVar RCV Id: RCV002676348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Val164Ile
CA414402068
NM_001122606.1:c.490G>A