Canonical Allele Identifier: PA2830123486
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1523977
ClinVar RCV Id: RCV002031377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gln238His
CA367400707
NM_033508.3:c.714G>T
CA367400708
NM_033508.3:c.714G>C