Canonical Allele Identifier: PA2828069573
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010556
ClinVar RCV Id: RCV001308198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Asn103Ser
CA410933856
NM_001362877.2:c.308A>G