Canonical Allele Identifier: PA645461108
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16140
ClinVar RCV Id: RCV000017520 RCV002513079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val456Met
CA257432
NM_033507.3:c.1366G>A