Canonical Allele Identifier: PA2830123536
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 421063
ClinVar RCV Id: RCV000485821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu255Gln
CA16618468
NM_033508.3:c.763G>C