Canonical Allele Identifier: PA2825581537
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174497
ClinVar RCV Id: RCV001528125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Met1Ile