Canonical Allele Identifier: PA2825684535
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_001122319.1:p.Glu1366Asp
CA404072805
NM_001128847.1:c.4098G>C
CA404072806
NM_001128847.1:c.4098G>T