Canonical Allele Identifier: PA279058
Gene: PDGFRB HGNC NCBI

Linked Data

ClinVar Variation Id: 217122
ClinVar RCV Id: RCV000200957 RCV001335958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002600.1:p.Pro584Arg
CA279057
NM_002609.3:c.1751C>G