Canonical Allele Identifier: PA916028486
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 830058
ClinVar RCV Id: RCV001030040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gly345Arg
CA340394369
NM_001330589.2:c.1033G>A
CA340394370
NM_001330589.2:c.1033G>C