Canonical Allele Identifier: PA915964854
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 291139
ClinVar RCV Id: RCV000278660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp741Val
CA10607034
NM_001079804.3:c.2222A>T