Canonical Allele Identifier: PA2825065423
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2066523
ClinVar RCV Id: RCV002966164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp330Cys
CA401364494
NM_000152.5:c.990G>C
CA401364495
NM_000152.5:c.990G>T