Canonical Allele Identifier: PA2825675869
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 939176
ClinVar RCV Id: RCV001208526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122316.1:p.Glu1399Asp
CA404072805
NM_001128844.1:c.4197G>C
CA404072806
NM_001128844.1:c.4197G>T