Canonical Allele Identifier: PA213718
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36177
ClinVar RCV Id: RCV000029840 RCV001642240 RCV003318495 RCV002444444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala379Glu
CA213717
NM_000162.5:c.1136C>A