Allele Registry

Canonical Allele Identifier: PA2825278866

Gene: SEMA3B HGNC NCBI

ClinVar RCV:

RCV003967348

ClinVar Variation:

3058923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005914.1:p.Thr414Ile	CA2413993 NM_001005914.3:c.1241C>T