Canonical Allele Identifier: PA916028523
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8959
ClinVar RCV Id: RCV000009519 RCV000202513 RCV001004160 RCV003317032 RCV002490348 RCV003473066 RCV003450624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Arg503Cys
CA120021
NM_001330589.2:c.1507C>T