Canonical Allele Identifier: PA2826974300
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_001304875.1:p.Lys372Asn
CA410913793
NM_001317946.2:c.1116G>C
CA410913795
NM_001317946.2:c.1116G>T