Canonical Allele Identifier: PA2827936931
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972776
ClinVar RCV Id: RCV001248986 RCV001879746 RCV003325991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala378Gly
CA367398802
NM_001354800.1:c.1133C>G