Canonical Allele Identifier: PA658828529
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 546099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asn181Lys
CA367401623
NM_033507.3:c.543T>G
CA367401624
NM_033507.3:c.543T>A