Canonical Allele Identifier: PA916028441
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 593649
ClinVar RCV Id: RCV000728751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Asn154Ser
CA22637719
NM_001330589.2:c.461A>G