Canonical Allele Identifier: PA915964850
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Val740Met
CA8815659
NM_001079804.3:c.2218G>A