Canonical Allele Identifier: PA915971917
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 639353
ClinVar RCV Id: RCV000792126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122321.1:p.Ser1449Asn
CA404073223
NM_001128849.1:c.4346G>A