Canonical Allele Identifier: PA2580490737
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2443137
ClinVar RCV Id: RCV003151529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe124Leu
CA367402213
NM_033507.3:c.372C>G
CA367402215
NM_033507.3:c.372C>A
CA367402221
NM_033507.3:c.370T>C