Canonical Allele Identifier: PA915963031
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 526578
ClinVar RCV Id: RCV000631139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Gly417Ala
CA966439
NM_000644.2:c.1250G>C