Canonical Allele Identifier: PA645477870
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Glu359del
CA8545070
NM_003079.5:c.1076_1078del