Canonical Allele Identifier: PA2829137110
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133432
ClinVar RCV Id: RCV003040930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374212.1:p.Thr3Ala
CA404053848
NM_001387283.1:c.7A>G