Canonical Allele Identifier: PA119238
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8031
ClinVar RCV Id: RCV000008496 RCV003231093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Glu31Val
CA119236
NM_003073.5:c.92A>T