Canonical Allele Identifier: PA2827937268
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 236014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser3Leu
CA10581499
NM_001354802.1:c.8C>T