Canonical Allele Identifier: PA2825673111
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 408637
ClinVar RCV Id: RCV000475490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122316.1:p.Gly15Val
CA16616097
NM_001128844.1:c.44G>T