Allele Registry

Canonical Allele Identifier: PA2826774968

Gene: SEMA3B HGNC NCBI

ClinVar RCV:

RCV003967348

ClinVar Variation:

3058923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276989.1:p.Thr415Ile	CA2413993 NM_001290060.2:c.1244C>T