Canonical Allele Identifier: PA134132
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44429
ClinVar RCV Id: RCV000037419 RCV000547615 RCV000675449 RCV002336129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054701.1:p.Thr158Ala
CA134126
NM_013995.2:c.472A>G