Canonical Allele Identifier: PA2579977349
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2682651
ClinVar RCV Id: RCV003481518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met37Thr
CA367403544
NM_000162.5:c.110T>C