Canonical Allele Identifier: PA915964169
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 522550
ClinVar RCV Id: RCV000625693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Pro75Arg
CA401360487
NM_001079804.3:c.224C>G