Canonical Allele Identifier: PA209487
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212263
ClinVar RCV Id: RCV000194966 RCV000515012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Lys363Glu
CA209485
NM_003073.5:c.1087A>G