Canonical Allele Identifier: PA658814487
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 528511
ClinVar RCV Id: RCV000633732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Asn328Asp
CA2922445
NM_006206.6:c.982A>G