Canonical Allele Identifier: PA915964719
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 501793
ClinVar RCV Id: RCV000597451 RCV001199859
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Amino-acid Alleles

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