Canonical Allele Identifier: PA2741997330
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2504386
ClinVar RCV Id: RCV003231847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu21Pro
CA367403809
NM_033507.3:c.62T>C