Canonical Allele Identifier: PA2827937055
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 521398
ClinVar RCV Id: RCV000623742 RCV001041035 RCV001824153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu442Lys
CA4239377
NM_001354800.1:c.1324G>A