Canonical Allele Identifier: PA916028429
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8953
ClinVar RCV Id: RCV000009510 RCV000185836 RCV000202499 RCV000194764 RCV000515252 RCV000662284 RCV000576571 RCV000624845 RCV001004157 RCV001813968 RCV003137507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Ser113Leu
CA254605
NM_001330589.2:c.338C>T