ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828069573
Gene: SMARCB1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1010556
ClinVar RCV Id:
RCV001308198
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001349806.1:p.Asn103Ser
CA410933856
NM_001362877.2:c.308A>G