Canonical Allele Identifier: PA2830123009
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2633338
ClinVar RCV Id: RCV003400047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Tyr124Asn
CA367402197
NM_033508.3:c.370T>A