Canonical Allele Identifier: PA2830122584
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1676825
ClinVar RCV Id: RCV002222321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gln17His
CA367403838
NM_033508.3:c.51G>T
CA367403840
NM_033508.3:c.51G>C