Canonical Allele Identifier: PA915964568
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 371235
ClinVar RCV Id: RCV000410896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met408Val
CA8815236
NM_001079804.3:c.1222A>G