Canonical Allele Identifier: PA2829638121
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 1763726
ClinVar RCV Id: RCV002447781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Ala341Val
CA356891629
NM_006206.6:c.1022C>T