Canonical Allele Identifier: PA2827937052
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435298
ClinVar RCV Id: RCV000499850 RCV003313087 RCV003482262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser441Leu
CA367397015
NM_001354800.1:c.1322C>T