Canonical Allele Identifier: PA133401
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 44021
ClinVar RCV Id: RCV000036996 RCV000770274 RCV001086084 RCV000724064 RCV003952426 RCV002345292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127835.2:p.Thr177Ser
CA133399
NM_001134363.3:c.529A>T