Canonical Allele Identifier: PA916049309
Gene: CPT1C HGNC NCBI
ClinVar RCV:
RCV000542129
ClinVar Variation:
476175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689572.1:p.Asn698Asp
CA9582408
NM_152359.3:c.2092A>G