ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826766002
Gene: SMARCA2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
68770
ClinVar RCV Id:
RCV000059671
RCV002255112
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001276326.1:p.Arg1047Pro
CA219890
NM_001289397.2:c.3140G>C