Canonical Allele Identifier: PA2829638712
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 1063386
ClinVar RCV Id: RCV001373216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006197.1:p.Asp583Glu
CA356893228
NM_006206.6:c.1749C>A
CA356893229
NM_006206.6:c.1749C>G