Canonical Allele Identifier: PA658669156
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389
ClinVar RCV Id: RCV000516995 RCV004527383
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe424Ser
CA367397256
NM_033507.3:c.1271T>C