Canonical Allele Identifier: PA2830123055
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1077171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe132Leu
CA367402113
NM_033508.3:c.396C>G
CA367402115
NM_033508.3:c.396C>A
CA367402122
NM_033508.3:c.394T>C