Canonical Allele Identifier: PA916039351
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389
ClinVar RCV Id: RCV000516995 RCV004527383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Phe86Ser
CA367397256
NM_001354801.1:c.257T>C