ClinGen Allele Registry
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Canonical Allele Identifier:
PA916043611
Gene: SMARCB1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000023124
RCV001017402
RCV001238882
ClinVar Variation:
30203
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001349806.1:p.Arg395His
CA129021
NM_001362877.2:c.1184G>A