Canonical Allele Identifier: PA2827936947
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 236014
ClinVar RCV Id: RCV000225001 RCV000420976 RCV003226260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser383Leu
CA10581499
NM_001354800.1:c.1148C>T