Allele Registry

Canonical Allele Identifier: PA2826974300

Gene: SMARCB1 HGNC NCBI

ClinVar Variation Id: 561114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304875.1:p.Lys372Asn	CA410913793 NM_001317946.2:c.1116G>C CA410913795 NM_001317946.2:c.1116G>T