Canonical Allele Identifier: PA2827937106
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val37Met
CA367398877
NM_001354801.1:c.109G>A