Allele Registry

Canonical Allele Identifier: PA161395

Gene: PDGFRA HGNC NCBI

ClinVar RCV:

RCV000034716

RCV000121780

RCV000326887

RCV000381487

RCV001011554

RCV002284181

ClinVar Variation:

41794

HGVS (amino-acid)	Matching Registered Transcripts
NP_006197.1:p.Ser478Pro	CA161393 NM_006206.6:c.1432T>C