Canonical Allele Identifier: PA215867
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 41798
ClinVar RCV Id: RCV000034720 RCV000230418 RCV001016840 RCV001146168 RCV003473260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.His966Arg
CA215865
NM_006206.6:c.2897A>G