Canonical Allele Identifier: PA2827486399
Gene: PLPBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1917998
ClinVar RCV Id: RCV002601750 RCV004065695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336275.1:p.Thr147Ser
CA4711233
NM_001349346.2:c.440C>G
CA370667933
NM_001349346.2:c.439A>T