Canonical Allele Identifier: PA213697
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36164
ClinVar RCV Id: RCV000029827 RCV002463591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe334_Val335delinsLeuMet
CA213696
NM_000162.5:c.1002_1003delinsAA