Canonical Allele Identifier: PA2825287034
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010556
ClinVar RCV Id: RCV001308198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Asn94Ser
CA410933856
NM_001007468.3:c.281A>G