Allele Registry

Canonical Allele Identifier: PA2826175042

Gene: SEMA4A HGNC NCBI

ClinVar RCV:

RCV000437436

ClinVar Variation:

384117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180229.1:p.Arg510Trp	CA16603466 NM_001193300.1:c.1528C>T