Canonical Allele Identifier: PA092066
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp746Ser
CA198797
NM_000152.5:c.2237G>C