Canonical Allele Identifier: PA913201960
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 617647
ClinVar RCV Id: RCV000754808 RCV002463738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asn241Asp
CA367400705
NM_033507.3:c.721A>G