Canonical Allele Identifier: PA2829638113
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 1433899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Val339Leu
CA2922446
NM_006206.6:c.1015G>T
CA356891617
NM_006206.6:c.1015G>C