Canonical Allele Identifier: PA658674844
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486508
ClinVar RCV Id: RCV000563096 RCV000638928 RCV003492106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Glu336Lys
CA8545117
NM_003079.5:c.1006G>A