Canonical Allele Identifier: PA2825287403
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039859
ClinVar RCV Id: RCV001343414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Lys355Met
CA410913819
NM_001007468.3:c.1064A>T