Canonical Allele Identifier: PA213708
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36172
ClinVar RCV Id: RCV000029835 RCV003493414 RCV003556089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile348Phe
CA213707
NM_000162.5:c.1042A>T