Canonical Allele Identifier: PA2830123793
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908614
ClinVar RCV Id: RCV001159191 RCV001159188 RCV001159189 RCV001159190
ClinVar Variation Id: 1338685
ClinVar RCV Id: RCV001818056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val373Leu
CA367398872
NM_033508.3:c.1117G>T
CA367398880
NM_033508.3:c.1117G>C