Canonical Allele Identifier: PA2830124000
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1763107
ClinVar RCV Id: RCV002434767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Lys419Asn
CA367397290
NM_033508.3:c.1257G>T
CA367397292
NM_033508.3:c.1257G>C