Canonical Allele Identifier: PA213728
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36182
ClinVar RCV Id: RCV000029845 RCV000493278 RCV001248970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala387Val
CA213727
NM_000162.5:c.1160C>T