Canonical Allele Identifier: PA645459501
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393454
ClinVar RCV Id: RCV000445500 RCV000992041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met42Thr
CA16609270
NM_033507.3:c.125T>C