Canonical Allele Identifier: PA645481954
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 420102
ClinVar RCV Id: RCV000486923 RCV001065031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr766Ser
CA8815680
NM_000152.5:c.2297A>C