Canonical Allele Identifier: PA2579978368
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578355
ClinVar RCV Id: RCV003326081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu146Arg
CA367401977
NM_000162.5:c.437T>G