Canonical Allele Identifier: PA2825067472
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Pro284Ser
CA859062
NM_000098.3:c.850C>T