Canonical Allele Identifier: PA2825679969
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 954832
ClinVar RCV Id: RCV001227359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122318.1:p.Ser17Phe
CA404053992
NM_001128846.2:c.50C>T