Canonical Allele Identifier: PA916029368
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_001334757.1:p.Asn353Asp
CA2922445
NM_001347828.2:c.1057A>G