Canonical Allele Identifier: PA2826174783
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1009849
ClinVar RCV Id: RCV001307400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180229.1:p.Gly33Glu
CA342834035
NM_001193300.1:c.98G>A