Canonical Allele Identifier: PA2579977266
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1763107
ClinVar RCV Id: RCV002434767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Lys420Asn
CA367397290
NM_000162.5:c.1260G>T
CA367397292
NM_000162.5:c.1260G>C