Canonical Allele Identifier: PA915962957
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 265986
ClinVar RCV Id: RCV000256372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Ser258Pro
CA10588921
NM_000644.2:c.772T>C