Allele Registry

Canonical Allele Identifier: PA2829216257

Gene: RBM41 HGNC NCBI

ClinVar RCV:

RCV004159549

ClinVar Variation:

2317283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001381050.1:p.Glu190Gly	CA413882070 NM_001394121.1:c.569A>G