Canonical Allele Identifier: PA891845641
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 579061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Leu37Val
CA8814789
NM_000152.5:c.109C>G