Canonical Allele Identifier: PA2579976997
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574163
ClinVar RCV Id: RCV003318528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met381Thr
CA367398764
NM_000162.5:c.1142T>C