Canonical Allele Identifier: PA2825358798
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2176267
ClinVar RCV Id: RCV002610145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Gly709Arg
CA6152093
NM_001031847.3:c.2125G>C
CA223365908
NM_001031847.3:c.2125G>A