Canonical Allele Identifier: PA2827936567
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg155Ser
CA367401896
NM_001354800.1:c.465G>T
CA367401898
NM_001354800.1:c.465G>C