Canonical Allele Identifier: PA113691
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2675759
ClinVar RCV Id: RCV003468225
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro768Arg
CA401324899
NM_000152.5:c.2303C>G