Canonical Allele Identifier: PA2829638650
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 1049734
ClinVar RCV Id: RCV001356217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Trp559_Val561delinsPhe
CA2499217252
NM_006206.6:c.1676_1681del