Canonical Allele Identifier: PA645481959
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 325793
ClinVar RCV Id: RCV000293486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr777Met
CA8815689
NM_000152.5:c.2330C>T