Canonical Allele Identifier: PA2579975472
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585925
ClinVar RCV Id: RCV000711784 RCV002463731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Tyr234Cys
CA367400748
NM_000162.5:c.701A>G