Canonical Allele Identifier: PA658674811
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486509
ClinVar RCV Id: RCV000570816 RCV000688644 RCV002476252 RCV003444603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Ala138Thr
CA8545247
NM_003079.5:c.412G>A