Canonical Allele Identifier: PA891845646
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 580689
ClinVar RCV Id: RCV000704307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala77Ser
CA401360496
NM_000152.5:c.229G>T