Canonical Allele Identifier: PA645481623
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 283894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg281Trp
CA8815025
NM_000152.5:c.841C>T