Canonical Allele Identifier: PA2580208639
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_001334757.1:p.Ser591Arg
CA356893106
NM_001347828.2:c.1771A>C
CA356893112
NM_001347828.2:c.1773C>A
CA356893113
NM_001347828.2:c.1773C>G