Canonical Allele Identifier: PA2826312967
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_001229849.1:p.Thr132Ser
CA409195805
NM_001242920.2:c.395C>G
CA409195809
NM_001242920.2:c.394A>T