ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827293673
Gene: SMARCC2
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317217.1:p.Asn398Thr
CA385349772
NM_001330288.2:c.1193A>C