Canonical Allele Identifier: PA658801309
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 526539
ClinVar RCV Id: RCV000631089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp741Glu
CA8815661
NM_000152.5:c.2223C>G
CA401324741
NM_000152.5:c.2223C>A