Allele Registry

Canonical Allele Identifier: PA2826175815

Gene: SEMA4A HGNC NCBI

ClinVar RCV:

RCV000437436

ClinVar Variation:

384117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180231.1:p.Arg378Trp	CA16603466 NM_001193302.1:c.1132C>T