Canonical Allele Identifier: PA2825581788
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449177
ClinVar RCV Id: RCV000522587 RCV000801420 RCV002358405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Glu334Gln
CA10505217
NM_001122606.1:c.1000G>C