Canonical Allele Identifier: PA2826765802
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 982400
ClinVar RCV Id: RCV001261978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276326.1:p.Asp510Gly
CA372782381
NM_001289397.2:c.1529A>G