Canonical Allele Identifier: PA2579974520
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val389Ala
CA367398657
NM_000162.5:c.1166T>C