Canonical Allele Identifier: PA213724
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180
ClinVar RCV Id: RCV000029843 RCV000517698 RCV002285137 RCV004527298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu386Pro
CA213723
NM_000162.5:c.1157T>C