Canonical Allele Identifier: PA2825287430
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 623977
ClinVar RCV Id: RCV000762051 RCV002458370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Thr372Arg
CA410914720
NM_001007468.3:c.1115C>G