Canonical Allele Identifier: PA2579979043
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile211Asn
CA367401285
NM_000162.5:c.632T>A