Canonical Allele Identifier: PA2827937168
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517
ClinVar RCV Id: RCV003084866 RCV003318514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg57Pro
CA367398581
NM_001354801.1:c.170G>C
CA2695203000
NM_001354801.1:c.170_171delinsCG