Canonical Allele Identifier: PA2827414367
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 2091950
ClinVar RCV Id: RCV003015864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334759.1:p.Ser579Arg
CA356893106
NM_001347830.2:c.1735A>C
CA356893112
NM_001347830.2:c.1737C>A
CA356893113
NM_001347830.2:c.1737C>G