Canonical Allele Identifier: PA2825064922
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1024896
ClinVar RCV Id: RCV001325135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro79Ser
CA8814819
NM_000152.5:c.235C>T