Canonical Allele Identifier: PA2825462774
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Thr739Ser
CA8815657
NM_001079803.3:c.2215A>T
CA401324731
NM_001079803.3:c.2216C>G