Canonical Allele Identifier: PA2828685038
Gene: PLXNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3215670
ClinVar RCV Id: RCV004509466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363809.1:p.Arg29His
CA10313665
NM_001376880.1:c.86G>A