Canonical Allele Identifier: PA2827333046
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 130890
ClinVar RCV Id: RCV000202475 RCV000591616 RCV003453044 RCV003453045 RCV003453046 RCV003453047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gly526Asp
CA347728
NM_001330589.2:c.1577G>A