Canonical Allele Identifier: PA2573200964
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431499
ClinVar RCV Id: RCV001940782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Trp351Cys
CA859115
NM_001330589.2:c.1053G>T
CA340394411
NM_001330589.2:c.1053G>C