Canonical Allele Identifier: PA2579975883
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser174Leu
CA367401688
NM_000162.5:c.521C>T