Canonical Allele Identifier: PA2827936594
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574158
ClinVar RCV Id: RCV003318523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr168Pro
CA367401755
NM_001354800.1:c.502A>C