Canonical Allele Identifier: PA213714
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36175
ClinVar RCV Id: RCV000029838 RCV002463593
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser375Phe
CA213713
NM_000162.5:c.1124C>T