Canonical Allele Identifier: PA2825066091
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1348299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asn635Asp
CA401369854
NM_000152.5:c.1903A>G