Canonical Allele Identifier: PA2825459727
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1024896
ClinVar RCV Id: RCV001325135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro79Ser
CA8814819
NM_001079803.3:c.235C>T