Canonical Allele Identifier: PA2827936757
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 418226
ClinVar RCV Id: RCV000482178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val253Ile
CA4239529
NM_001354800.1:c.757G>A