Canonical Allele Identifier: PA096468
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr209Met
CA367401309
NM_000162.5:c.626C>T