Canonical Allele Identifier: PA2579976566
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1346275
ClinVar RCV Id: RCV002029930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser151Tyr
CA367401935
NM_000162.5:c.452C>A