Canonical Allele Identifier: PA2579981502
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679544
ClinVar RCV Id: RCV002227423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp205Val
CA367401343
NM_000162.5:c.614A>T