Allele Registry

Canonical Allele Identifier: PA2741856957

Gene: SEMA3B HGNC NCBI

ClinVar RCV:

RCV003967348

ClinVar Variation:

3058923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276992.1:p.Thr72Ile	CA2413993 NM_001290063.2:c.215C>T