Canonical Allele Identifier: PA2825682657
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 939176
ClinVar RCV Id: RCV001208526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122318.1:p.Glu1369Asp
CA404072805
NM_001128846.2:c.4107G>C
CA404072806
NM_001128846.2:c.4107G>T