Canonical Allele Identifier: PA134145
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44431
ClinVar RCV Id: RCV000037421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Leu19Arg
CA134140
NM_002294.3:c.56T>G