Canonical Allele Identifier: PA2741868520
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701457
ClinVar RCV Id: RCV003549685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Lys382Asn
CA410913820
NM_001362877.2:c.1146G>C
CA410913821
NM_001362877.2:c.1146G>T