Canonical Allele Identifier: PA2579982027
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2581305
ClinVar RCV Id: RCV003331710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg392Ser
CA367398628
NM_000162.5:c.1174C>A