Canonical Allele Identifier: PA2827936798
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447421
ClinVar RCV Id: RCV000516582 RCV002463708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp274His
CA367400487
NM_001354800.1:c.820G>C