Canonical Allele Identifier: PA2825898308
Gene: RFX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2511383
ClinVar RCV Id: RCV004282456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139136.2:p.Gln212Leu
CA1806431
NM_001145664.2:c.635A>T