Canonical Allele Identifier: PA1139744785
Gene: CPT1C HGNC NCBI

Linked Data

ClinVar Variation Id: 542768
ClinVar RCV Id: RCV000653259 RCV003907915 RCV004025900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365411.1:p.Pro709Ala
CA9582404
NM_001378482.1:c.2125C>G