Canonical Allele Identifier: PA2579978369
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2740810
ClinVar RCV Id: RCV003575875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu144Val
CA367401998
NM_000162.5:c.430C>G