Canonical Allele Identifier: PA2827410186
Gene: PDGFRA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334757.1:p.His119Gln
CA2922263
NM_001347828.2:c.357C>A
CA356888775
NM_001347828.2:c.357C>G