Allele Registry

Canonical Allele Identifier: PA645502361

Gene: FREM2 HGNC NCBI

ClinVar RCV:

RCV000399828

RCV000873182

RCV001111920

RCV003957487

ClinVar Variation:

287581

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Met711Ile	CA6954549 NM_207361.6:c.2133G>A CA387888182 NM_207361.6:c.2133G>C CA387888183 NM_207361.6:c.2133G>T