Canonical Allele Identifier: PA2825064812
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1015157
ClinVar RCV Id: RCV001313981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser9Phe
CA401359935
NM_000152.5:c.26C>T