Allele Registry

Canonical Allele Identifier: PA357879

Gene: FREM1 HGNC NCBI

ClinVar RCV:

RCV000203291

RCV000249912

RCV000289080

RCV002057046

ClinVar Variation:

218939

HGVS (amino-acid)	Matching Registered Transcripts
NP_659403.4:p.Gly465Ala	CA339661 NM_144966.7:c.1394G>C