Canonical Allele Identifier: PA916028455
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 645541
ClinVar RCV Id: RCV000799641 RCV002495062 RCV003453658 RCV003453659 RCV003453660 RCV003453661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Arg219Gln
CA22638136
NM_001330589.2:c.656G>A