Canonical Allele Identifier: PA916043603
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 561114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Lys381Asn
CA410913793
NM_001362877.2:c.1143G>C
CA410913795
NM_001362877.2:c.1143G>T