Canonical Allele Identifier: PA2580490755
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1803244
ClinVar RCV Id: RCV002466914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe134Val
CA367402121
NM_033507.3:c.400T>G