Canonical Allele Identifier: PA2579977073
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1464253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met224Thr
CA367401149
NM_000162.5:c.671T>C