Canonical Allele Identifier: PA645481989
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 325794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg891Pro
CA10640874
NM_000152.5:c.2672G>C