Canonical Allele Identifier: PA1139735383
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 985725
ClinVar RCV Id: RCV001266778 RCV002463797 RCV003558780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly85Ser
CA367398357
NM_001354803.2:c.253G>A