Canonical Allele Identifier: PA2827936880
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2581175
ClinVar RCV Id: RCV003331580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val338Met
CA367399707
NM_001354800.1:c.1012G>A