Canonical Allele Identifier: PA891855227
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585913
ClinVar RCV Id: RCV000711764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg44Pro
CA367403448
NM_033507.3:c.131G>C