Canonical Allele Identifier: PA916028485
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376799
ClinVar RCV Id: RCV000427828 RCV000667275 RCV000763959 RCV001079544 RCV002289546 RCV003387839 RCV004022260 RCV003957893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Met342Thr
CA859108
NM_001330589.2:c.1025T>C