Canonical Allele Identifier: PA2573176446
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1396416
ClinVar RCV Id: RCV001887422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Pro6Ser
CA401359883
NM_001079804.3:c.16C>T