Canonical Allele Identifier: PA658801234
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 526537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg178Cys
CA8814888
NM_000152.5:c.532C>T