Canonical Allele Identifier: PA096199
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256304
ClinVar RCV Id: RCV001663646 RCV003318508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys382Tyr
CA367398751
NM_000162.5:c.1145G>A