Canonical Allele Identifier: PA2825286981
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532973
ClinVar RCV Id: RCV000639926 RCV001012689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Val57Met
CA322595527
NM_001007468.3:c.169G>A