Canonical Allele Identifier: PA645481997
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 325795
ClinVar RCV Id: RCV000265557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser918Phe
CA8815848
NM_000152.5:c.2753C>T