Canonical Allele Identifier: PA658678521
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456419
ClinVar RCV Id: RCV000537422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg11Trp
CA8814759
NM_000152.5:c.31C>T