Canonical Allele Identifier: PA152956
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129145
ClinVar RCV Id: RCV000117132 RCV000497903 RCV001844042 RCV003343641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr206Pro
CA152955
NM_000162.5:c.616A>C