Canonical Allele Identifier: PA2826999136
Gene: SEMA3F HGNC NCBI

Linked Data

ClinVar Variation Id: 982049
ClinVar RCV Id: RCV001374679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305729.1:p.Ala621Ser
CA352902099
NM_001318800.2:c.1861G>T