Canonical Allele Identifier: PA2825067354
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368806
ClinVar RCV Id: RCV001867681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Asn222Ser
CA859027
NM_000098.3:c.665A>G