Canonical Allele Identifier: PA1139731489
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_001334757.1:p.Asp616Asn
CA356893280
NM_001347828.2:c.1846G>A