Canonical Allele Identifier: PA2579974468
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1303093
ClinVar RCV Id: RCV001756592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val406Met
CA367398367
NM_000162.5:c.1216G>A