Allele Registry

Canonical Allele Identifier: PA2829558880

Gene: SEMA3B HGNC NCBI

ClinVar RCV:

RCV003967348

ClinVar Variation:

3058923

HGVS (amino-acid)	Matching Registered Transcripts
NP_004627.1:p.Thr415Ile	CA2413993 NM_004636.4:c.1244C>T