Canonical Allele Identifier: PA658829931
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 561114
ClinVar RCV Id: RCV000680105 RCV001533135 RCV001543528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Lys363Asn
CA410913793
NM_003073.5:c.1089G>C
CA410913795
NM_003073.5:c.1089G>T