Canonical Allele Identifier: PA2826973812
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 826242
ClinVar RCV Id: RCV001025002 RCV001362384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Asp21Asn
CA410930807
NM_001317946.2:c.61G>A