Canonical Allele Identifier: PA2579978803
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709688
ClinVar RCV Id: RCV002289503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His50Leu
CA367403390
NM_000162.5:c.149A>T