Canonical Allele Identifier: PA2741868032
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578348
ClinVar RCV Id: RCV003326074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val52Glu
CA367398869
NM_001354803.2:c.155T>A