Canonical Allele Identifier: PA113064
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 189013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp645His
CA274256
NM_000152.5:c.1933G>C