Canonical Allele Identifier: PA2579981669
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3026940
ClinVar RCV Id: RCV003887333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp198Ala
CA367401419
NM_000162.5:c.593A>C