Canonical Allele Identifier: PA2828683289
Gene: PLXNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3215670
ClinVar RCV Id: RCV004509466
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363798.1:p.Arg29His
CA10313665
NM_001376869.1:c.86G>A