Allele Registry

Canonical Allele Identifier: PA2826775039

Gene: SEMA3B HGNC NCBI

ClinVar RCV:

RCV003967348

ClinVar Variation:

3058923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276990.1:p.Thr420Ile	CA2413993 NM_001290061.1:c.1259C>T