Canonical Allele Identifier: PA2828685985
Gene: PLXNB2 HGNC NCBI
ClinVar RCV:
RCV004509466
ClinVar Variation:
3215670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363815.1:p.Arg29His
CA10313665
NM_001376886.1:c.86G>A