Canonical Allele Identifier: PA213738
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36187
ClinVar RCV Id: RCV000029850 RCV001288976 RCV002345255 RCV003234925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg403Gly
CA213737
NM_000162.5:c.1207C>G