Canonical Allele Identifier: PA2827936647
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136523
ClinVar RCV Id: RCV003037219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val200Leu
CA367401396
NM_001354800.1:c.598G>T
CA367401397
NM_001354800.1:c.598G>C