Canonical Allele Identifier: PA2579977866
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 235097
ClinVar RCV Id: RCV000223803 RCV003556284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu30Pro
CA10581225
NM_000162.5:c.89T>C