Canonical Allele Identifier: PA2573097841
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338409
ClinVar RCV Id: RCV001817780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His142Gln
CA367402023
NM_033507.3:c.426C>G
CA367402025
NM_033507.3:c.426C>A