Canonical Allele Identifier: PA2741997349
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664358
ClinVar RCV Id: RCV003445456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met38Val
CA367403551
NM_033507.3:c.112A>G