Canonical Allele Identifier: PA658674850
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463412
ClinVar RCV Id: RCV000532044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Thr361Met
CA8545068
NM_003079.5:c.1082C>T