Canonical Allele Identifier: PA2826175240
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 951711
ClinVar RCV Id: RCV001223689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180230.1:p.Ser70Gly
CA1154946
NM_001193301.1:c.208A>G