Canonical Allele Identifier: PA2825067526
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492726
ClinVar RCV Id: RCV001981182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Arg316Ser
CA340394186
NM_000098.3:c.948G>C
CA340394187
NM_000098.3:c.948G>T