Canonical Allele Identifier: PA2830123675
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16136
ClinVar RCV Id: RCV001288185 RCV000017516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly298Arg
CA126212
NM_033508.3:c.892G>C