Canonical Allele Identifier: PA2827936970
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asn391Lys
CA367398630
NM_001354800.1:c.1173C>G
CA367398633
NM_001354800.1:c.1173C>A