Canonical Allele Identifier: PA2827937341
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709730
ClinVar RCV Id: RCV002290072 RCV003395445 RCV003445164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.His44Tyr
CA367397245
NM_001354802.1:c.130C>T