Canonical Allele Identifier: PA161413
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 135017
ClinVar RCV Id: RCV000121786 RCV000461163 RCV001022920 RCV003128582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Thr16Ser
CA161411
NM_006206.6:c.46A>T