Canonical Allele Identifier: PA2579980661
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys382Ser
CA367398745
NM_000162.5:c.1145G>C
CA367398756
NM_000162.5:c.1144T>A