Canonical Allele Identifier: PA2825287412
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 985428
ClinVar RCV Id: RCV001266328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Asp360Val
CA410913974
NM_001007468.3:c.1079A>T