Canonical Allele Identifier: PA2826312955
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_001229849.1:p.Val69Leu
CA409198694
NM_001242920.2:c.205G>T
CA409198701
NM_001242920.2:c.205G>C