Canonical Allele Identifier: PA2825581760
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2709050
ClinVar RCV Id: RCV003510732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116078.1:p.Met303Leu
CA414400309
NM_001122606.1:c.907A>T
CA414400310
NM_001122606.1:c.907A>C