Canonical Allele Identifier: PA114768
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1107
ClinVar RCV Id: RCV000001166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Arg1147Gly
CA114767
NM_000642.3:c.3439A>G