Canonical Allele Identifier: PA2573248623
Gene: PLTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1469132
ClinVar RCV Id: RCV001961425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006218.1:p.Thr227Ser
CA409195805
NM_006227.4:c.680C>G
CA409195809
NM_006227.4:c.679A>T