Canonical Allele Identifier: PA2827936436
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338576
ClinVar RCV Id: RCV001817947 RCV002285503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala53Val
CA367403352
NM_001354800.1:c.158C>T