Canonical Allele Identifier: PA915971923
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 824813
ClinVar RCV Id: RCV001022333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122321.1:p.Asp1450Gly
CA404073250
NM_001128849.1:c.4349A>G