Canonical Allele Identifier: PA2741997622
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met252Ile
CA367400628
NM_033507.3:c.756G>T
CA367400629
NM_033507.3:c.756G>A
CA367400630
NM_033507.3:c.756G>C