Canonical Allele Identifier: PA2827411620
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 1763726
ClinVar RCV Id: RCV002447781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334758.1:p.Ala341Val
CA356891629
NM_001347829.2:c.1022C>T