Canonical Allele Identifier: PA2580490703
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700673
ClinVar RCV Id: RCV002285551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met42Arg
CA367403469
NM_033507.3:c.125T>G