Canonical Allele Identifier: PA916028490
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 92428
ClinVar RCV Id: RCV000078115 RCV000202443 RCV000444353 RCV000578014 RCV003453001 RCV003456002 RCV003982874 RCV003452999 RCV003453000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Phe352Cys
CA145733
NM_001330589.2:c.1055T>G