Canonical Allele Identifier: PA2827936539
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338409
ClinVar RCV Id: RCV001817780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.His141Gln
CA367402023
NM_001354800.1:c.423C>G
CA367402025
NM_001354800.1:c.423C>A