Canonical Allele Identifier: PA915964919
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Arg837Cys
CA8815777
NM_001079804.3:c.2509C>T