Canonical Allele Identifier: PA2829374428
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521589
ClinVar RCV Id: RCV002046335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Asn307Asp
CA414400281
NM_002294.3:c.919A>G