Canonical Allele Identifier: PA2579978731
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024422
ClinVar RCV Id: RCV003883458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile130Asn
CA367402147
NM_000162.5:c.389T>A