Canonical Allele Identifier: PA2827936933
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21076
ClinVar RCV Id: RCV000020165 RCV003325943 RCV003556055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala378Val
CA341585
NM_001354800.1:c.1133C>T