Canonical Allele Identifier: PA2825065669
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1354481
ClinVar RCV Id: RCV001866447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met440Thr
CA8815259
NM_000152.5:c.1319T>C