Canonical Allele Identifier: PA1139670922
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 929166
ClinVar RCV Id: RCV001194238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met363Val
CA401364927
NM_001079804.3:c.1087A>G