Canonical Allele Identifier: PA916039393
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36178
ClinVar RCV Id: RCV002281721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Met59Arg
CA213719
NM_001354803.2:c.176T>G