Canonical Allele Identifier: PA2826766053
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521357
ClinVar RCV Id: RCV000623090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276326.1:p.Val1140Gly
CA372788932
NM_001289397.2:c.3419T>G