Canonical Allele Identifier: PA2741997492
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_277042.1:p.Thr169Asn
CA367401747
NM_033507.3:c.506C>A