Canonical Allele Identifier: PA891845639
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 570091
ClinVar RCV Id: RCV000690873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Leu26Arg
CA401360183
NM_000152.5:c.77T>G