Canonical Allele Identifier: PA2830122992
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2443137
ClinVar RCV Id: RCV003151529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe122Leu
CA367402213
NM_033508.3:c.366C>G
CA367402215
NM_033508.3:c.366C>A
CA367402221
NM_033508.3:c.364T>C