Canonical Allele Identifier: PA2827937281
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Asn11Lys
CA367398630
NM_001354802.1:c.33C>G
CA367398633
NM_001354802.1:c.33C>A