Canonical Allele Identifier: PA2827936658
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36234
ClinVar Variation Id: 1807283
ClinVar RCV Id: RCV002475240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp205Glu
CA213812
NM_001354800.1:c.615C>G
CA367401342
NM_001354800.1:c.615C>A