Canonical Allele Identifier: PA2830123520
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 810090
ClinVar RCV Id: RCV000998793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys251Phe
CA367400622
NM_033508.3:c.752G>T