Canonical Allele Identifier: PA2579976390
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe419Leu
CA367397305
NM_000162.5:c.1257C>G
CA367397306
NM_000162.5:c.1257C>A
CA367397316
NM_000162.5:c.1255T>C