Canonical Allele Identifier: PA2825065503
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1359350
ClinVar RCV Id: RCV001904391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr366Ser
CA401364945
NM_000152.5:c.1097A>C