Canonical Allele Identifier: PA658800489
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 526592
ClinVar RCV Id: RCV000631153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Cys399Tyr
CA341345151
NM_000642.3:c.1196G>A