Canonical Allele Identifier: PA2827486958
Gene: PLPBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1934485
ClinVar RCV Id: RCV002638735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336277.1:p.Phe13Ser
CA370666759
NM_001349348.2:c.38T>C