Canonical Allele Identifier: PA645459529
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36226
ClinVar RCV Id: RCV000029889 RCV002463598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala177Gly
CA213796
NM_033507.3:c.530C>G