Canonical Allele Identifier: PA113698
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1700765
ClinVar RCV Id: RCV002275756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro913Arg
CA401327099
NM_000152.5:c.2738C>G