Canonical Allele Identifier: PA2573176938
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1483591
ClinVar RCV Id: RCV001998851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Tyr928His
CA401327369
NM_001079804.3:c.2782T>C