Canonical Allele Identifier: PA916028510
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 550475
ClinVar RCV Id: RCV000665230 RCV001868201 RCV003451633 RCV003451634 RCV003451635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Gln468His
CA340395614
NM_001330589.2:c.1404G>C
CA340395615
NM_001330589.2:c.1404G>T