Canonical Allele Identifier: PA2825699850
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718466
ClinVar RCV Id: RCV002304905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122321.1:p.Ser1484Phe
CA404073974
NM_001128849.1:c.4451C>T