Canonical Allele Identifier: PA1139748917
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972806
ClinVar RCV Id: RCV001249060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly194Arg
CA4239599
NM_033507.3:c.580G>C
CA367401514
NM_033507.3:c.580G>A