Canonical Allele Identifier: PA916039390
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447382
ClinVar RCV Id: RCV000518241 RCV003318500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala57Gly
CA367398793
NM_001354803.2:c.170C>G