Canonical Allele Identifier: PA916004920
Gene: RFX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 92042
ClinVar RCV Id: RCV000122599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193620.1:p.Pro68Ser
CA232409
NM_001206691.2:c.202C>T