Canonical Allele Identifier: PA2828781861
Gene: CPT1C HGNC NCBI

Linked Data

ClinVar Variation Id: 476175
ClinVar RCV Id: RCV000542129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365414.1:p.Asn687Asp
CA9582408
NM_001378485.1:c.2059A>G