Canonical Allele Identifier: PA2825358803
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2860095
ClinVar RCV Id: RCV003752452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Gly710Arg
CA381625770
NM_001031847.3:c.2128G>C
CA381625771
NM_001031847.3:c.2128G>A