Canonical Allele Identifier: PA116163
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 3361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180230.1:p.Phe350Cys
CA116162
NM_001193301.1:c.1049T>G