Canonical Allele Identifier: PA915957206
Gene: RFX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 292619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020774.1:p.Gly14Arg
CA1089972
NM_001025603.2:c.40G>A
CA341947427
NM_001025603.2:c.40G>C