Canonical Allele Identifier: PA2741932641
Gene: SEMA4D HGNC NCBI

Linked Data

ClinVar Variation Id: 3060636
ClinVar RCV Id: RCV003984615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006369.3:p.Ala327Thr
CA5118507
NM_006378.3:c.979G>A