Canonical Allele Identifier: PA2825684568
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739941
ClinVar RCV Id: RCV002332278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122319.1:p.Ala1386Ser
CA404073276
NM_001128847.1:c.4156G>T