Canonical Allele Identifier: PA2830122836
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36210
ClinVar RCV Id: RCV000029873 RCV002465491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg84Trp
CA213773
NM_033508.3:c.250A>T