Canonical Allele Identifier: PA2579974509
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435300
ClinVar RCV Id: RCV000499682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val389Leu
CA367398665
NM_000162.5:c.1165G>C