Canonical Allele Identifier: PA2827937147
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36182
ClinVar RCV Id: RCV000029845 RCV000493278 RCV001248970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala50Val
CA213727
NM_001354801.1:c.149C>T