Canonical Allele Identifier: PA2827937179
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1303093
ClinVar RCV Id: RCV001756592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val69Met
CA367398367
NM_001354801.1:c.205G>A