Canonical Allele Identifier: PA2827936972
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1301416
ClinVar RCV Id: RCV001732837 RCV003326000 RCV003900855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg392Gly
CA367398625
NM_001354800.1:c.1174C>G