Canonical Allele Identifier: PA2827937332
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1763107
ClinVar RCV Id: RCV002434767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Lys40Asn
CA367397290
NM_001354802.1:c.120G>T
CA367397292
NM_001354802.1:c.120G>C