Canonical Allele Identifier: PA2825463534
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1048589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Tyr928Cys
CA401327377
NM_001079803.3:c.2783A>G