Canonical Allele Identifier: PA2741940513
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2898726
ClinVar RCV Id: RCV003622014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054701.1:p.Arg152Lys
CA414402205
NM_013995.2:c.455G>A