ClinGen Allele Registry
Allele Registry
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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