Canonical Allele Identifier: PA915964415
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 556117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Pro266Ser
CA401363495
NM_001079804.3:c.796C>T