Allele Registry

Canonical Allele Identifier: PA2827412271

Gene: PDGFRA HGNC NCBI

ClinVar Variation Id: 459033

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334758.1:p.Met642Ile	CA356893638 NM_001347829.2:c.1926G>A CA356893639 NM_001347829.2:c.1926G>C CA356893640 NM_001347829.2:c.1926G>T