Canonical Allele Identifier: PA2573227696
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403668
ClinVar RCV Id: RCV001909170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Ser389Pro
CA8545053
NM_003079.5:c.1165T>C