Canonical Allele Identifier: PA219897
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 68773
ClinVar RCV Id: RCV000059679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003061.3:p.Ala1188Pro
CA219896
NM_003070.5:c.3562G>C