Canonical Allele Identifier: PA2827937265
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser3Trp
CA367398735
NM_001354802.1:c.8C>G