Canonical Allele Identifier: PA2830123077
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2740810
ClinVar RCV Id: RCV003575875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu143Val
CA367401998
NM_033508.3:c.427C>G