Canonical Allele Identifier: PA2827936809
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36260
ClinVar RCV Id: RCV000029923 RCV000992065 RCV002463613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp278Val
CA213856
NM_001354800.1:c.833A>T