Canonical Allele Identifier: PA2827936774
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1479681
ClinVar RCV Id: RCV002009866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala259Asp
CA367400580
NM_001354800.1:c.776C>A