Canonical Allele Identifier: PA2741997464
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2740810
ClinVar RCV Id: RCV003575875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu145Val
CA367401998
NM_033507.3:c.433C>G