Canonical Allele Identifier: PA2825067274
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1486923
ClinVar RCV Id: RCV002497967 RCV002033420 RCV003453926 RCV003453925 RCV003456268 RCV003453924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Glu174Gln
CA340392451
NM_000098.3:c.520G>C