Canonical Allele Identifier: PA349863
Gene: SMARCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219351
ClinVar RCV Id: RCV000205753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003066.2:p.Thr1193Pro
CA349860
NM_003075.5:c.3577A>C