Canonical Allele Identifier: PA096477
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16134
ClinVar RCV Id: RCV000020167 RCV000498792 RCV001269032 RCV002362586 RCV003147295 RCV003147296 RCV003883118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr228Met
CA260620
NM_000162.5:c.683C>T