Canonical Allele Identifier: PA2825691829
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739941
ClinVar RCV Id: RCV002332278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122320.1:p.Ala1386Ser
CA404073276
NM_001128848.2:c.4156G>T