Canonical Allele Identifier: PA645436799
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291339
ClinVar RCV Id: RCV000306756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Gln989Arg
CA966948
NM_000642.3:c.2966A>G