Allele Registry

Canonical Allele Identifier: PA645502423

Gene: FREM2 HGNC NCBI

ClinVar RCV:

RCV000348468

RCV000767220

RCV000767221

ClinVar Variation:

284704

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Arg2167Trp	CA6955578 NM_207361.6:c.6499C>T