Allele Registry

Canonical Allele Identifier: PA645507003

Gene: SEMA4A HGNC NCBI

ClinVar RCV:

RCV000437436

ClinVar Variation:

384117

HGVS (amino-acid)	Matching Registered Transcripts
NP_071762.2:p.Arg510Trp	CA16603466 NM_022367.4:c.1528C>T