Canonical Allele Identifier: PA915964739
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 286469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Thr614Met
CA8815496
NM_001079804.3:c.1841C>T