Canonical Allele Identifier: PA101115
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523331
ClinVar RCV Id: RCV000626609 RCV000696870 RCV000711320 RCV001196658 RCV001731819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Tyr479Phe
CA859201
NM_000098.3:c.1436A>T