Canonical Allele Identifier: PA916039366
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429500
ClinVar RCV Id: RCV000494422 RCV001290675 RCV002489206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg67Gln
CA367396940
NM_001354802.1:c.200G>A