Canonical Allele Identifier: PA2827409136
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 240369
ClinVar RCV Id: RCV000227020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334756.1:p.Val332Asp
CA10582239
NM_001347827.2:c.995T>A