Canonical Allele Identifier: PA2828684923
Gene: PLXNB2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363808.1:p.Arg503Gln
CA10313191
NM_001376879.1:c.1508G>A