Canonical Allele Identifier: PA658807936
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532249
ClinVar RCV Id: RCV000638926 RCV002406373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Asn356Ser
CA8545071
NM_003079.5:c.1067A>G