Canonical Allele Identifier: PA2499237736
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023390
ClinVar RCV Id: RCV001323420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091896.1:p.Pro92Ser
CA8706537
NM_001098426.2:c.274C>T