Canonical Allele Identifier: PA2826312986
Gene: PLTP HGNC NCBI
ClinVar RCV:
RCV003546167
ClinVar Variation:
2716331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229849.1:p.Arg209Lys
CA9883685
NM_001242920.2:c.626G>A