Canonical Allele Identifier: PA2580490744
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1704058
ClinVar RCV Id: RCV002281393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu129Asp
CA367402163
NM_033507.3:c.387G>T
CA367402164
NM_033507.3:c.387G>C