Canonical Allele Identifier: PA2827937013
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36188
ClinVar RCV Id: RCV000029851 RCV000711759 RCV001248969 RCV003398573 RCV004017269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Lys414Glu
CA213739
NM_001354800.1:c.1240A>G