Canonical Allele Identifier: PA2830123118
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068510
ClinVar RCV Id: RCV003993702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe149Leu
CA367401941
NM_033508.3:c.447C>G
CA367401942
NM_033508.3:c.447C>A
CA367401948
NM_033508.3:c.445T>C