Canonical Allele Identifier: PA2828781856
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_001365414.1:p.Pro676Ala
CA9582404
NM_001378485.1:c.2026C>G