Canonical Allele Identifier: PA2830123781
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val366Leu
CA367398995
NM_033508.3:c.1096G>T
CA367398997
NM_033508.3:c.1096G>C