Canonical Allele Identifier: PA2827313619
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202828
ClinVar RCV Id: RCV002648191 RCV002648192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317368.1:p.Asp38Ala
CA292954745
NM_001330439.1:c.113A>C