Canonical Allele Identifier: PA2827936529
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1489454
ClinVar RCV Id: RCV001978311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile130Phe
CA367402148
NM_001354800.1:c.388A>T