Canonical Allele Identifier: PA2827936521
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585920
ClinVar RCV Id: RCV000711773 RCV002464030 RCV003993678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile126Thr
CA367402185
NM_001354800.1:c.377T>C