Canonical Allele Identifier: PA2573296321
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1676825
ClinVar RCV Id: RCV002222321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gln19His
CA367403838
NM_033507.3:c.57G>T
CA367403840
NM_033507.3:c.57G>C