Canonical Allele Identifier: PA2827937277
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val9Ala
CA367398657
NM_001354802.1:c.26T>C