ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA162161
Gene: SMARCB1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000122071
RCV000456257
RCV000563927
RCV001150088
RCV001150089
ClinVar Variation:
135257
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003064.2:p.Met1Val