ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828069472
Gene: SMARCB1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
8031
ClinVar RCV Id:
RCV000008496
RCV003231093
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001349806.1:p.Glu31Val
CA119236
NM_001362877.2:c.92A>T