Canonical Allele Identifier: PA2828236443
Gene: RFX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2522643
ClinVar RCV Id: RCV004297770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354437.1:p.Ala58Thr
CA1806426
NM_001367508.1:c.172G>A