Canonical Allele Identifier: PA1139725660
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 839921
ClinVar RCV Id: RCV001041791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Met438Lys
CA859174
NM_001330589.2:c.1313T>A