Canonical Allele Identifier: PA1139725451
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 856543
ClinVar RCV Id: RCV001062023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Ser267Pro
CA340393754
NM_001330589.2:c.799T>C