Canonical Allele Identifier: PA2830122746
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2097728
ClinVar RCV Id: RCV003018951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr48Ser
CA367403400
NM_033508.3:c.143C>G
CA367403406
NM_033508.3:c.142A>T