Canonical Allele Identifier: PA206548
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp124Asn
CA206547
NM_000162.5:c.370G>A