Canonical Allele Identifier: PA2826312946
Gene: PLTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1529887
ClinVar RCV Id: RCV002080119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229849.1:p.His16Arg
CA9884031
NM_001242920.2:c.47A>G