Canonical Allele Identifier: PA2573296586
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1691788
ClinVar RCV Id: RCV002255216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala174Pro
CA367401703
NM_033507.3:c.520G>C