Canonical Allele Identifier: PA2827936703
Gene: GCK HGNC NCBI
ClinVar RCV:
RCV003330053
ClinVar Variation:
2580858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val226Gly
CA367401120
NM_001354800.1:c.677T>G