Canonical Allele Identifier: PA2579978916
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447386
ClinVar RCV Id: RCV000516548 RCV004527381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly410Asp
CA367398309
NM_000162.5:c.1229G>A