Canonical Allele Identifier: PA2579977076
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2505485
ClinVar RCV Id: RCV003234753
ClinVar Variation Id: 2505486
ClinVar RCV Id: RCV003234754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met210Val
CA367401305
NM_000162.5:c.628A>G
CA2018007653
NM_000162.5:c.627_628delinsAG