Canonical Allele Identifier: PA2825042272
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807285
ClinVar RCV Id: RCV002475242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp29Tyr
CA367403666
NM_000162.5:c.85G>T