Canonical Allele Identifier: PA658819806
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 522430
ClinVar RCV Id: RCV000625570 RCV002463723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe331Ser
CA367399791
NM_033507.3:c.992T>C