Canonical Allele Identifier: PA2579976846
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1352737
ClinVar RCV Id: RCV002049532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe84Ser
CA367402973
NM_000162.5:c.251T>C