Canonical Allele Identifier: PA2829642349
Gene: PLTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1500998
ClinVar RCV Id: RCV002042701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006218.1:p.Val164Leu
CA409198694
NM_006227.4:c.490G>T
CA409198701
NM_006227.4:c.490G>C