Canonical Allele Identifier: PA106406
Gene: PDGFRB HGNC NCBI

Linked Data

ClinVar Variation Id: 39589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002600.1:p.Arg987Trp
CA343799
NM_002609.3:c.2959C>T