Allele Registry

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This migration is underway but taking longer than originally estimated.

Canonical Allele Identifier: PA2827937142

Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36179

ClinVar RCV Id: RCV000029842 RCV002463594

ClinVar Variation Id: 2065408

ClinVar RCV Id: RCV002958450

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Gly48Arg	CA213721 NM_001354801.1:c.142G>A CA367398717 NM_001354801.1:c.142G>C