Canonical Allele Identifier: PA2827937247
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068512
ClinVar RCV Id: RCV003993704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala117Val
CA367396861
NM_001354801.1:c.350C>T