Canonical Allele Identifier: PA2826766033
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320261
ClinVar RCV Id: RCV001775434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276326.1:p.Ala1102Gly
CA372788650
NM_001289397.2:c.3305C>G