Canonical Allele Identifier: PA2827937152
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val52Ala
CA367398657
NM_001354801.1:c.155T>C