Allele Registry

Canonical Allele Identifier: PA915964719

Gene: GAA HGNC NCBI

ClinVar Allele:

493217

ClinVar RCV:

RCV000597451

RCV001199859

ClinVar Variation:

501793

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073272.1:p.Ser601Trp	CA294896338 NM_001079804.3:c.1802C>G