Canonical Allele Identifier: PA2830123079
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 451640
ClinVar RCV Id: RCV000523438 RCV002464024
ClinVar Variation Id: 2921032
ClinVar RCV Id: RCV003740508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu143Pro
CA367401995
NM_033508.3:c.428T>C
CA2695202965
NM_033508.3:c.428_429delinsCT