Canonical Allele Identifier: PA2579975616
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2682649
ClinVar RCV Id: RCV003481516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr168Asn
CA367401747
NM_000162.5:c.503C>A