Canonical Allele Identifier: PA2828683651
Gene: PLXNB2 HGNC NCBI
ClinVar RCV:
RCV004509424
ClinVar Variation:
3215628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363800.1:p.Arg503Gln
CA10313191
NM_001376871.1:c.1508G>A