Canonical Allele Identifier: PA2827936966
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435300
ClinVar RCV Id: RCV000499682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val389Leu
CA367398665
NM_001354800.1:c.1165G>C