Canonical Allele Identifier: PA2827936399
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 431973
ClinVar RCV Id: RCV000497478 RCV000503648 RCV000788107 RCV003403150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg36Trp
CA4239720
NM_001354800.1:c.106C>T