Canonical Allele Identifier: PA2579976942
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met41Thr
CA16609270
NM_000162.5:c.122T>C