Canonical Allele Identifier: PA2827937021
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1763107
ClinVar RCV Id: RCV002434767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Lys420Asn
CA367397290
NM_001354800.1:c.1260G>T
CA367397292
NM_001354800.1:c.1260G>C