Canonical Allele Identifier: PA213783
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36217
ClinVar RCV Id: RCV001248972 RCV002271379 RCV003565386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly147Asp
CA213782
NM_000162.5:c.440G>A