Canonical Allele Identifier: PA2580282074
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1751150
ClinVar RCV Id: RCV002358137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Pro405Leu
CA399360784
NM_003079.5:c.1214C>T