Canonical Allele Identifier: PA2573186238
Gene: PLTP HGNC NCBI
ClinVar RCV:
RCV002042701
ClinVar Variation:
1500998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229850.1:p.Val76Leu
CA409198694
NM_001242921.1:c.226G>T
CA409198701
NM_001242921.1:c.226G>C