Canonical Allele Identifier: PA891866302
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 133374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334756.1:p.Thr782Met
CA156465
NM_001347827.2:c.2345C>T