Canonical Allele Identifier: PA279948
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 219179
ClinVar RCV Id: RCV000203555 RCV002463661 RCV004527370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp344Tyr
CA279947
NM_000162.5:c.1030G>T