Canonical Allele Identifier: PA2579976762
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1077171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe133Leu
CA367402113
NM_000162.5:c.399C>G
CA367402115
NM_000162.5:c.399C>A
CA367402122
NM_000162.5:c.397T>C