Canonical Allele Identifier: PA2825581540
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765425
ClinVar RCV Id: RCV002376348 RCV003100077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Cys3Ser
CA335014954
NM_001122606.1:c.8G>C
CA414398121
NM_001122606.1:c.7T>A