Canonical Allele Identifier: PA2573296611
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1447652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu185Pro
CA367401589
NM_033507.3:c.554T>C