Canonical Allele Identifier: PA2827937102
Gene: GCK HGNC NCBI
ClinVar RCV:
RCV003326073
ClinVar Variation:
2578347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Cys34Tyr
CA367398935
NM_001354801.1:c.101G>A