Canonical Allele Identifier: PA2827936675
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile211Asn
CA367401285
NM_001354800.1:c.632T>A