Canonical Allele Identifier: PA2827937033
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585912
ClinVar RCV Id: RCV000711762 RCV002463456 RCV004527395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val427Gly
CA367397199
NM_001354800.1:c.1280T>G