Canonical Allele Identifier: PA2579980622
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1704058
ClinVar RCV Id: RCV002281393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu128Asp
CA367402163
NM_000162.5:c.384G>T
CA367402164
NM_000162.5:c.384G>C