Canonical Allele Identifier: PA2828781616
Gene: CPT1C HGNC NCBI
ClinVar RCV:
RCV000542129
ClinVar Variation:
476175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365413.1:p.Asn698Asp
CA9582408
NM_001378484.1:c.2092A>G