Canonical Allele Identifier: PA2827937105
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_001341730.1:p.Val37Leu
CA367398872
NM_001354801.1:c.109G>T
CA367398880
NM_001354801.1:c.109G>C