Canonical Allele Identifier: PA2830122485
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1320655
ClinVar RCV Id: RCV001776634 RCV003313230 RCV003401708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser442Trp
CA367397017
NM_033507.3:c.1325C>G