Canonical Allele Identifier: PA341588
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077
ClinVar RCV Id: RCV000518294 RCV003318494 RCV000020166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg397Leu
CA341587
NM_000162.5:c.1190G>T