Canonical Allele Identifier: PA2829411244
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701457
ClinVar RCV Id: RCV003549685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Lys364Asn
CA410913820
NM_003073.5:c.1092G>C
CA410913821
NM_003073.5:c.1092G>T