Canonical Allele Identifier: PA2499263253
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043383
ClinVar RCV Id: RCV001347486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Ser389Trp
CA399361055
NM_003079.5:c.1166C>G