Canonical Allele Identifier: PA2828829636
Gene: RFX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 292619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366347.1:p.Gly14Arg
CA1089972
NM_001379418.1:c.40G>A
CA341947427
NM_001379418.1:c.40G>C