Canonical Allele Identifier: PA2825066321
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 938987
ClinVar RCV Id: RCV001208306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr739Ala
CA8815658
NM_000152.5:c.2215A>G