Canonical Allele Identifier: PA2826974312
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 985428
ClinVar RCV Id: RCV001266328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Asp378Val
CA410913974
NM_001317946.2:c.1133A>T