Canonical Allele Identifier: PA2827936944
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Cys382Ser
CA367398745
NM_001354800.1:c.1145G>C
CA367398756
NM_001354800.1:c.1144T>A