Canonical Allele Identifier: PA2827936616
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735014
ClinVar RCV Id: RCV003555339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asn180Ser
CA367401627
NM_001354800.1:c.539A>G