Canonical Allele Identifier: PA2825461278
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 167112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Tyr407His
CA234047
NM_001079803.3:c.1219T>C