Canonical Allele Identifier: PA234049
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 167112
ClinVar RCV Id: RCV000153288 RCV001326695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr407His
CA234047
NM_000152.5:c.1219T>C