Canonical Allele Identifier: PA2829374200
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174497
ClinVar RCV Id: RCV001528125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Met1Ile
CA414398143
NM_002294.3:c.3G>A
CA414398145
NM_002294.3:c.3G>C
CA414398148
NM_002294.3:c.3G>T