Canonical Allele Identifier: PA645481954
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 420102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr766Ser
CA8815680
NM_000152.5:c.2297A>C