Canonical Allele Identifier: PA2825065496
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2413164
ClinVar RCV Id: RCV003110174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met363Ile
CA401364930
NM_000152.5:c.1089G>C
CA401364931
NM_000152.5:c.1089G>T
CA401364932
NM_000152.5:c.1089G>A