Canonical Allele Identifier: PA113735
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4026
ClinVar RCV Id: RCV000004241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser529Val
CA116604
NM_000152.5:c.1585_1586delinsGT