Canonical Allele Identifier: PA2579977129
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447409
ClinVar RCV Id: RCV000518379 RCV002463702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met197Thr
CA367401431
NM_000162.5:c.590T>C