Canonical Allele Identifier: PA915964913
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 580968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Glu835Asp
CA8815776
NM_001079804.3:c.2505G>C
CA401326009
NM_001079804.3:c.2505G>T