Canonical Allele Identifier: PA213716
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36176
ClinVar RCV Id: RCV000029839 RCV000518143 RCV001818186 RCV002321490 RCV003325945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg377His
CA213715
NM_000162.5:c.1130G>A