Canonical Allele Identifier: PA916028445
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529863
ClinVar RCV Id: RCV000635365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Leu170Arg
CA22637761
NM_001330589.2:c.509T>G
CA658795466
NM_001330589.2:c.509_510delinsGC