Canonical Allele Identifier: PA645460250
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36248
ClinVar RCV Id: RCV000029911 RCV003556090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met236Thr
CA213834
NM_033507.3:c.707T>C