Canonical Allele Identifier: PA2829374215
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 650063
ClinVar RCV Id: RCV000805144 RCV002440711
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Pro10Leu
CA10505375
NM_002294.3:c.29C>T