Canonical Allele Identifier: PA2499266128
Gene: SEMA3F HGNC NCBI

Linked Data

ClinVar Variation Id: 982049
ClinVar RCV Id: RCV001374679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004177.3:p.Ala652Ser
CA352902099
NM_004186.3:c.1954G>T