Canonical Allele Identifier: PA645481957
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 392862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp772Cys
CA16607903
NM_000152.5:c.2316G>T
CA401324924
NM_000152.5:c.2316G>C