Canonical Allele Identifier: PA891848987
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 573127
ClinVar RCV Id: RCV000694711 RCV002360763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Glu408Lys
CA399360740
NM_003079.5:c.1222G>A