Canonical Allele Identifier: PA2825923918
Gene: SEMA7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1687038
ClinVar RCV Id: RCV002248475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139501.1:p.Arg134Trp
CA7657257
NM_001146029.2:c.400C>T