Canonical Allele Identifier: PA2827937309
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1300949
ClinVar RCV Id: RCV001733092 RCV002222722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val28Met
CA367398343
NM_001354802.1:c.82G>A