Canonical Allele Identifier: PA133398
Gene: RBM20 HGNC NCBI

Linked Data

ClinVar Variation Id: 44020
ClinVar RCV Id: RCV000036995 RCV000465419 RCV000770273 RCV000248470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127835.2:p.Pro173Thr
CA133396
NM_001134363.3:c.517C>A