Canonical Allele Identifier: PA2825686737
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 643858
ClinVar RCV Id: RCV000797658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122320.1:p.Thr11Ser
CA404053920
NM_001128848.2:c.31A>T
CA404053924
NM_001128848.2:c.32C>G