Canonical Allele Identifier: PA2573200982
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386943
ClinVar RCV Id: RCV001905905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.His372Leu
CA340394549
NM_001330589.2:c.1115A>T
CA2573131912
NM_001330589.2:c.1115_1116delinsTT