Allele Registry

Canonical Allele Identifier: PA119238

Gene: SMARCB1 HGNC NCBI

ClinVar RCV:

RCV000008496

RCV003231093

ClinVar Variation:

8031

HGVS (amino-acid)	Matching Registered Transcripts
NP_003064.2:p.Glu31Val	CA119236 NM_003073.5:c.92A>T