Canonical Allele Identifier: PA2829411250
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 985428
ClinVar RCV Id: RCV001266328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Asp369Val
CA410913974
NM_003073.5:c.1106A>T