Canonical Allele Identifier: PA2827937153
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435300
ClinVar RCV Id: RCV000499682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val52Leu
CA367398665
NM_001354801.1:c.154G>C