Canonical Allele Identifier: PA2827937338
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675
ClinVar RCV Id: RCV002443287 RCV002285553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg42Trp
CA367397271
NM_001354802.1:c.124C>T