Canonical Allele Identifier: PA2579982527
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2867056
ClinVar RCV Id: RCV003700530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg422Gly
CA367397273
NM_000162.5:c.1264C>G