Canonical Allele Identifier: PA2827937079
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143
ClinVar RCV Id: RCV000017525 RCV001818166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala456Val
CA257433
NM_001354800.1:c.1367C>T