Canonical Allele Identifier: PA2579979067
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 431972
ClinVar RCV Id: RCV000498428 RCV002285343 RCV002350106 RCV003228938 RCV003403149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile189Thr
CA367401550
NM_000162.5:c.566T>C