Canonical Allele Identifier: PA2825689279
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780249
ClinVar RCV Id: RCV002407793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122320.1:p.Ile599Phe
CA404064842
NM_001128848.2:c.1795A>T