Canonical Allele Identifier: PA2827936929
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16145
ClinVar RCV Id: RCV000017527 RCV003325941 RCV002513080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala378Thr
CA126216
NM_001354800.1:c.1132G>A