Allele Registry

Canonical Allele Identifier: PA2826766060

Gene: SMARCA2 HGNC NCBI

ClinVar Variation Id: 430455

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276326.1:p.Phe1146Leu	CA372788968 NM_001289397.2:c.3436T>C CA372788972 NM_001289397.2:c.3438T>A CA372788973 NM_001289397.2:c.3438T>G