Canonical Allele Identifier: PA645500746
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 432859
ClinVar Variation Id: 2839685
ClinVar RCV Id: RCV003599544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127835.2:p.Trp707Arg
CA378371941
NM_001134363.3:c.2119T>A
CA378371945
NM_001134363.3:c.2119T>C