Canonical Allele Identifier: PA251407
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127835.2:p.Pro638Leu
CA251405
NM_001134363.3:c.1913C>T
CA645568266
NM_001134363.3:c.1912_1913delinsTT