Allele Registry

Canonical Allele Identifier: PA100005

Gene: FREM1 HGNC NCBI

ClinVar Allele:

17028

ClinVar RCV:

RCV000002066

RCV000059637

RCV003987307

ClinVar Variation:

1989

HGVS (amino-acid)	Matching Registered Transcripts
NP_659403.4:p.Arg649Trp	CA115305 NM_144966.7:c.1945C>T