Canonical Allele Identifier: PA2829638732
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 965392
ClinVar RCV Id: RCV001239830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Asp591Asn
CA356893280
NM_006206.6:c.1771G>A