Canonical Allele Identifier: PA213811
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36233
ClinVar RCV Id: RCV000029896 RCV000711779 RCV003445084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met202Thr
CA213810
NM_000162.5:c.605T>C