Canonical Allele Identifier: PA112785
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2675751
ClinVar RCV Id: RCV003461594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala486Pro
CA401366835
NM_000152.5:c.1456G>C