Canonical Allele Identifier: PA2573256272
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1518488
ClinVar RCV Id: RCV002021782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054701.1:p.Cys153Tyr
CA414402194
NM_013995.2:c.458G>A