Allele Registry

Canonical Allele Identifier: PA916065900

Gene: SEMA4A HGNC NCBI

ClinVar RCV:

RCV000946503

RCV001097416

RCV001097417

ClinVar Variation:

767708

HGVS (amino-acid)	Matching Registered Transcripts
NP_071762.2:p.Gly7Asp	CA1154880 NM_022367.4:c.20G>A