Canonical Allele Identifier: PA916043559
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 575245
ClinVar RCV Id: RCV000697410 RCV003163216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.His185Gln
CA410935396
NM_001362877.2:c.555C>A
CA410935397
NM_001362877.2:c.555C>G