Canonical Allele Identifier: PA2827313846
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_001317369.1:p.Gly50Val
CA400601657
NM_001330440.2:c.149G>T