Canonical Allele Identifier: PA915989373
Gene: CUTC HGNC NCBI

Linked Data

ClinVar Variation Id: 298428
ClinVar RCV Id: RCV000359052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057044.2:p.Arg3Thr
CA10629652
NM_015960.3:c.8G>C