Canonical Allele Identifier: PA2826974290
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 580796
ClinVar RCV Id: RCV000997886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Thr366Ile
CA410913532
NM_001317946.2:c.1097C>T