Canonical Allele Identifier: PA349862
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_001123892.1:p.Thr1131Pro
CA349860
NM_001130420.3:c.3391A>C