Canonical Allele Identifier: PA2827410925
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 135017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334758.1:p.Thr16Ser
CA161411
NM_001347829.2:c.46A>T