Canonical Allele Identifier: PA2573200889
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423552
ClinVar RCV Id: RCV001928918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val264Leu
CA340393723
NM_001330589.2:c.790G>C
CA340393725
NM_001330589.2:c.790G>T