Canonical Allele Identifier: PA2825287057
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2566863
ClinVar RCV Id: RCV003306779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Pro108Ser
CA410934073
NM_001007468.3:c.322C>T