Canonical Allele Identifier: PA2830122097
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1727652
ClinVar RCV Id: RCV002325992 RCV003102308 RCV003330331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg378Ser
CA367398819
NM_033507.3:c.1132C>A