Canonical Allele Identifier: PA2827937182
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2702306
ClinVar RCV Id: RCV003577301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Gly70Arg
CA367398355
NM_001354801.1:c.208G>C