Canonical Allele Identifier: PA2830122773
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Pro58Ser
CA213767
NM_033508.3:c.172C>T