Canonical Allele Identifier: PA2830123895
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asn390Lys
CA367398630
NM_033508.3:c.1170C>G
CA367398633
NM_033508.3:c.1170C>A