Canonical Allele Identifier: PA916028479
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447221
ClinVar RCV Id: RCV000517266 RCV000549753 RCV003962430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Asn311Ser
CA859085
NM_001330589.2:c.932A>G