Canonical Allele Identifier: PA2830123488
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136514
ClinVar RCV Id: RCV003037216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asn239Thr
CA367400703
NM_033508.3:c.716A>C