Canonical Allele Identifier: PA113309
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly615Arg
CA273955
NM_000152.5:c.1843G>A
CA401369596
NM_000152.5:c.1843G>C