Canonical Allele Identifier: PA1139671392
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 849167
ClinVar RCV Id: RCV001053072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asn520Ser
CA401367197
NM_001079804.3:c.1559A>G