Canonical Allele Identifier: PA2741997506
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735014
ClinVar RCV Id: RCV003555339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asn181Ser
CA367401627
NM_033507.3:c.542A>G