Allele Registry

Canonical Allele Identifier: PA1139716089

Gene: SMARCE1 HGNC NCBI

ClinVar Variation Id: 951720

ClinVar RCV Id: RCV001223698

ClinVar Variation Id: 1351659

ClinVar RCV Id: RCV002044895

HGVS (amino-acid)	Matching Registered Transcripts
NP_003070.3:p.Thr363Ser	CA399361492 NM_003079.5:c.1088C>G CA399361496 NM_003079.5:c.1087A>T CA1139665513 NM_003079.5:c.1086_1087delinsAT