ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA349861
Gene: SMARCC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
219351
ClinVar RCV Id:
RCV000205753
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_620706.1:p.Thr1109Pro
CA349860
NM_139067.4:c.3325A>C