Canonical Allele Identifier: PA2828685908
Gene: PLXNB2 HGNC NCBI
ClinVar RCV:
RCV004509431
ClinVar Variation:
3215635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363814.1:p.Arg820Cys
CA10312739
NM_001376885.1:c.2458C>T