Canonical Allele Identifier: PA092128
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 285197
ClinVar RCV Id: RCV000403113 RCV001049848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr766Cys
CA8815679
NM_000152.5:c.2297A>G