Canonical Allele Identifier: PA199138
Gene: CPT1C HGNC NCBI

Linked Data

ClinVar Variation Id: 189198
ClinVar RCV Id: RCV000169633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186682.1:p.Arg37Cys
CA199135
NM_001199753.2:c.109C>T