Canonical Allele Identifier: PA2830122646
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36173
ClinVar RCV Id: RCV000029836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg35Pro
CA213709
NM_033508.3:c.104G>C