Canonical Allele Identifier: PA2825065655
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 951262
ClinVar RCV Id: RCV001223131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg436Trp
CA8815255
NM_000152.5:c.1306C>T