Canonical Allele Identifier: PA645500687
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 418454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127835.2:p.Tyr681Cys
CA5688663
NM_001134363.3:c.2042A>G