Canonical Allele Identifier: PA2825462899
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 420102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Tyr766Ser
CA8815680
NM_001079803.3:c.2297A>C