Canonical Allele Identifier: PA2580490699
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801853
ClinVar RCV Id: RCV002464672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val34Gly
CA367403603
NM_033507.3:c.101T>G