Canonical Allele Identifier: PA2499249772
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020752
ClinVar RCV Id: RCV001320383 RCV002486273 RCV003456216 RCV003449913 RCV003449914 RCV003449915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Phe475Tyr
CA22639808
NM_001330589.2:c.1424T>A