Canonical Allele Identifier: PA2825287386
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 850717
ClinVar RCV Id: RCV001054947 RCV002400314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Pro342Leu
CA410913376
NM_001007468.3:c.1025C>T