Canonical Allele Identifier: PA1139670548
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 972389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp163Val
CA8814880
NM_001079804.3:c.488A>T