Canonical Allele Identifier: PA916065918
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 3361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071762.2:p.Phe350Cys
CA116162
NM_022367.4:c.1049T>G