Canonical Allele Identifier: PA916039362
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435298
ClinVar RCV Id: RCV000499850 RCV003313087 RCV003482262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser61Leu
CA367397015
NM_001354802.1:c.182C>T