Canonical Allele Identifier: PA645459504
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429796
ClinVar RCV Id: RCV000493595 RCV002465692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu46Pro
CA367403437
NM_033507.3:c.137T>C