Allele Registry

Canonical Allele Identifier: PA2825287402

Gene: SMARCB1 HGNC NCBI

ClinVar Variation Id: 561114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001007469.1:p.Lys354Asn	CA410913793 NM_001007468.3:c.1062G>C CA410913795 NM_001007468.3:c.1062G>T