Canonical Allele Identifier: PA2579982899
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393451
ClinVar RCV Id: RCV000445484 RCV000517148 RCV000754803 RCV002393068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg250Cys
CA16609268
NM_000162.5:c.748C>T