Canonical Allele Identifier: PA2827937020
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe419Leu
CA367397305
NM_001354800.1:c.1257C>G
CA367397306
NM_001354800.1:c.1257C>A
CA367397316
NM_001354800.1:c.1255T>C