Allele Registry

Canonical Allele Identifier: PA645502409

Gene: FREM2 HGNC NCBI

ClinVar RCV:

RCV000276477

ClinVar Variation:

311997

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Val1893Ile	CA6955317 NM_207361.6:c.5677G>A