Canonical Allele Identifier: PA2827936780
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211075
ClinVar RCV Id: RCV000193049 RCV002463660 RCV002478669 RCV003765221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp262Asn
CA206279
NM_001354800.1:c.784G>A