Canonical Allele Identifier: PA2827936692
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36241
ClinVar RCV Id: RCV000029904 RCV000711781 RCV002371787 RCV003155041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu221Lys
CA213824
NM_001354800.1:c.661G>A