Canonical Allele Identifier: PA2579982322
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735014
ClinVar RCV Id: RCV003555339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asn180Ser
CA367401627
NM_000162.5:c.539A>G