Allele Registry

Canonical Allele Identifier: PA645502427

Gene: FREM2 HGNC NCBI

ClinVar Allele:

319645

ClinVar RCV:

RCV000329779

RCV000593390

RCV002487379

ClinVar Variation:

312013

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Ala2393Thr	CA6955779 NM_207361.6:c.7177G>A