Canonical Allele Identifier: PA2828236464
Gene: RFX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2522643
ClinVar RCV Id: RCV004297770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354438.1:p.Ala58Thr
CA1806426
NM_001367509.1:c.172G>A