Canonical Allele Identifier: PA2580282040
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428099
ClinVar RCV Id: RCV003117070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Gly388Asp
CA290547498
NM_003079.5:c.1163G>A