Canonical Allele Identifier: PA2827937207
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447388
ClinVar RCV Id: RCV000518696 RCV003325961 RCV003419896 RCV002463697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Phe82Leu
CA367397305
NM_001354801.1:c.246C>G
CA367397306
NM_001354801.1:c.246C>A
CA367397316
NM_001354801.1:c.244T>C