Canonical Allele Identifier: PA2825287407
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1343154
ClinVar RCV Id: RCV001843755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Arg357Gly
CA410913856
NM_001007468.3:c.1069C>G