Canonical Allele Identifier: PA2579981023
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 418228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp363Asn
CA16618466
NM_000162.5:c.1087G>A