Canonical Allele Identifier: PA2828682631
Gene: PLXNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3215635
ClinVar RCV Id: RCV004509431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363793.1:p.Arg820Cys
CA10312739
NM_001376864.1:c.2458C>T