Canonical Allele Identifier: PA2579976381
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571660
ClinVar RCV Id: RCV003313370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe419Val
CA367397313
NM_000162.5:c.1255T>G