Canonical Allele Identifier: PA2830122035
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802685
ClinVar RCV Id: RCV002465963 RCV003326018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val368Leu
CA367398995
NM_033507.3:c.1102G>T
CA367398997
NM_033507.3:c.1102G>C