Canonical Allele Identifier: PA658802190
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Trp746Ser
CA198797
NM_001079803.3:c.2237G>C