Canonical Allele Identifier: PA2580141201
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946191
ClinVar RCV Id: RCV002658722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091896.1:p.Gly98Val
CA400601657
NM_001098426.2:c.293G>T