Canonical Allele Identifier: PA2826974010
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_001304875.1:p.His176Gln
CA410935396
NM_001317946.2:c.528C>A
CA410935397
NM_001317946.2:c.528C>G