Canonical Allele Identifier: PA2579975004
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1444770
ClinVar RCV Id: RCV001955981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Tyr61Asn
CA367403298
NM_000162.5:c.181T>A