Allele Registry

Canonical Allele Identifier: PA2828442899

Gene: SEMA4A HGNC NCBI

ClinVar RCV:

RCV000437436

ClinVar Variation:

384117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357497.1:p.Arg411Trp	CA16603466 NM_001370568.1:c.1231C>T