Canonical Allele Identifier: PA2825042364
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 546099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asn180Lys
CA367401623
NM_000162.5:c.540T>G
CA367401624
NM_000162.5:c.540T>A