Canonical Allele Identifier: PA2827936702
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36243
ClinVar RCV Id: RCV000029906 RCV000255932 RCV000825615 RCV002477021 RCV003155042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val226Met
CA213827
NM_001354800.1:c.676G>A