Canonical Allele Identifier: PA2741899525
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2888216
ClinVar RCV Id: RCV003638437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Asp407Tyr
CA8545044
NM_003079.5:c.1219G>T