Canonical Allele Identifier: PA2579977335
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met381Lys
CA367398767
NM_000162.5:c.1142T>A