Canonical Allele Identifier: PA2579975608
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1490297
ClinVar RCV Id: RCV001978541 RCV003446980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr168Ile
CA367401750
NM_000162.5:c.503C>T