Canonical Allele Identifier: PA2825065602
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 650087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser410Phe
CA8815238
NM_000152.5:c.1229C>T