Canonical Allele Identifier: PA2827937262
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Cys2Ser
CA367398745
NM_001354802.1:c.5G>C
CA367398756
NM_001354802.1:c.4T>A