Canonical Allele Identifier: PA658675141
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 464334
ClinVar RCV Id: RCV000548946 RCV004023978 RCV003459234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Thr232Met
CA10146033
NM_003073.5:c.695C>T