Canonical Allele Identifier: PA2829411236
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782663
ClinVar RCV Id: RCV002410696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Thr357Ala
CA410913524
NM_003073.5:c.1069A>G