Canonical Allele Identifier: PA2580175986
Gene: PLTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1981886
ClinVar RCV Id: RCV002766481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229850.1:p.Ser31Ala
CA315612921
NM_001242921.1:c.91T>G