Canonical Allele Identifier: PA2741997479
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628364
ClinVar RCV Id: RCV003397219 RCV003565665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg156Ser
CA367401896
NM_033507.3:c.468G>T
CA367401898
NM_033507.3:c.468G>C