Canonical Allele Identifier: PA2830124013
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709730
ClinVar RCV Id: RCV002290072 RCV003395445 RCV003445164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His423Tyr
CA367397245
NM_033508.3:c.1267C>T