Canonical Allele Identifier: PA2825287060
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Leu111Phe
CA10145894
NM_001007468.3:c.331C>T