Canonical Allele Identifier: PA2827937381
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233995
ClinVar RCV Id: RCV004527571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly88Ser
CA367398315
NM_001354803.2:c.262G>A