Canonical Allele Identifier: PA2825067590
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431499
ClinVar RCV Id: RCV001940782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Trp351Cys
CA859115
NM_000098.3:c.1053G>T
CA340394411
NM_000098.3:c.1053G>C