Canonical Allele Identifier: PA2825358792
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1935202
ClinVar RCV Id: RCV002623034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Ser708Gly
CA381625781
NM_001031847.3:c.2122A>G