Canonical Allele Identifier: PA2825065313
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1763158
ClinVar RCV Id: RCV002434818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp279Cys
CA401363642
NM_000152.5:c.837G>T
CA401363644
NM_000152.5:c.837G>C