Canonical Allele Identifier: PA2827937377
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val67Ala
CA367398657
NM_001354803.2:c.200T>C