Allele Registry

Canonical Allele Identifier: PA100025

Gene: FREM1 HGNC NCBI

ClinVar RCV:

RCV000002067

RCV000059639

RCV003987308

ClinVar Variation:

1990

HGVS (amino-acid)	Matching Registered Transcripts
NP_659403.4:p.Gly1440Ser	CA115306 NM_144966.7:c.4318G>A