Canonical Allele Identifier: PA658801338
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 526515
ClinVar RCV Id: RCV000631053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr911Met
CA294858598
NM_000152.5:c.2732C>T