ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645459090
Gene: SMARCB1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
265393
ClinVar RCV Id:
RCV000255465
RCV001782753
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003064.2:p.Arg366Cys
CA10588715
NM_003073.5:c.1096C>T