Canonical Allele Identifier: PA2579981953
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136514
ClinVar RCV Id: RCV003037216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asn240Thr
CA367400703
NM_000162.5:c.719A>C