Canonical Allele Identifier: PA2828236439
Gene: RFX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2511383
ClinVar RCV Id: RCV004282456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354437.1:p.Gln41Leu
CA1806431
NM_001367508.1:c.122A>T