Canonical Allele Identifier: PA199137
Gene: CPT1C HGNC NCBI

Linked Data

ClinVar Variation Id: 189198
ClinVar RCV Id: RCV000169633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186681.1:p.Arg37Cys
CA199135
NM_001199752.3:c.109C>T