Canonical Allele Identifier: PA213722
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36179
ClinVar RCV Id: RCV000029842 RCV002463594
ClinVar Variation Id: 2065408
ClinVar RCV Id: RCV002958450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly385Arg
CA213721
NM_000162.5:c.1153G>A
CA367398717
NM_000162.5:c.1153G>C