Canonical Allele Identifier: PA2579975143
Gene: GCK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val226Gly
CA367401120
NM_000162.5:c.677T>G