Canonical Allele Identifier: PA2580229361
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg72Pro
CA367398581
NM_001354803.2:c.215G>C
CA2695203000
NM_001354803.2:c.215_216delinsCG