Canonical Allele Identifier: PA2827413191
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 135017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334759.1:p.Thr29Ser
CA161411
NM_001347830.2:c.85A>T