Canonical Allele Identifier: PA658675654
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 463967
ClinVar RCV Id: RCV000554631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Arg173Cys
CA6152641
NM_001876.4:c.517C>T