Canonical Allele Identifier: PA645459508
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Pro60Ser
CA213767
NM_033507.3:c.178C>T