Canonical Allele Identifier: PA916022126
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 582394
ClinVar RCV Id: RCV001342433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Asp92Gly
CA10145889
NM_001317946.2:c.275A>G