Canonical Allele Identifier: PA2741997420
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2881307
ClinVar RCV Id: RCV003715883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr119Ser
CA367402572
NM_033507.3:c.356C>G
CA367402575
NM_033507.3:c.355A>T