Canonical Allele Identifier: PA2827936636
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 426122
ClinVar RCV Id: RCV000490143 RCV000754816 RCV002350083 RCV002496884 RCV003318499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg191Trp
CA367401530
NM_001354800.1:c.571C>T