Canonical Allele Identifier: PA211316
Gene: PDGFRB HGNC NCBI

Linked Data

ClinVar Variation Id: 135650
ClinVar RCV Id: RCV000128554 RCV001560202 RCV001795218 RCV003764848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002600.1:p.Arg695Cys
CA211315
NM_002609.3:c.2083C>T