Canonical Allele Identifier: PA2826974077
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 340912
ClinVar RCV Id: RCV000299341 RCV000337956 RCV000559614 RCV001024873 RCV001789772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Ala212Thr
CA10145992
NM_001317946.2:c.634G>A